Johns Hopkins University (JHU) - SciVal Experts v3.6

148 Publications

This is a list of publications by this researcher, listed chronologically starting with the most recent first. New publications appear in this list weekly. The source of publications for this application is PubMed, so only PubMed publications are included.

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1.
2013

Alison Dolce; Bruria Ben-Zeev; Sakkubai Naidu; Eric H Kossoff

Rett syndrome and epilepsy: an update for child neurologists.
Pediatric neurology 2013;48(5):337-45.
2.
2013

Hussein Daoud; Martine Tétreault; William Gibson; Kether Guerrero; Ana Cohen; Janina Gburek-Augustat; Matthis Synofzik; Bernard Brais; Cathy A Stevens; Rocio Sanchez-Carpintero; et al.

Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism.
Journal of medical genetics 2013;50(3):194-7.
3.
2012

Sakkubai Naidu; Doris D M Lin

Advances in the diagnosis of leukoencephalopathies.
Expert opinion on medical diagnostics 2012;6(4):259-73.
4.
2012

Daniel Flint; Rong Li; Lital S Webster; Sakkubai Naidu; Edwin Kolodny; Alan Percy; Marjo van der Knaap; James M Powers; John F Mantovani; Josef Ekstein; et al.

Splice site, frameshift, and chimeric GFAP mutations in Alexander disease.
Human mutation 2012;33(7):1141-8.
5.
2012

James Robert Brašić; Genila Bibat; Anil Kumar; Yun Zhou; John Hilton; Marybeth E Yablonski; Ahmet Semih Dogan; Maria Rita Guevara; Massoud Stephane; Michael Johnston; et al.

Correlation of the vesicular acetylcholine transporter densities in the striata to the clinical abilities of women with Rett syndrome.
Synapse (New York, N.Y.) 2012;66(6):471-82.
6.
2012

Beverley H Anderson; Paul R Kasher; Josephine Mayer; Marcin Szynkiewicz; Emma M Jenkinson; Sanjeev S Bhaskar; Jill E Urquhart; Sarah B Daly; Jonathan E Dickerson; James O'Sullivan; et al.

Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus.
Nature genetics 2012;44(3):338-42.
7.
2012

W E Kaufmann; E Tierney; C A Rohde; M C Suarez-Pedraza; M A Clarke; C F Salorio; G Bibat; I Bukelis; D Naram; D C Lanham; et al.

Social impairments in Rett syndrome: characteristics and relationship with clinical severity.
Journal of intellectual disability research : JIDR 2012;56(3):233-47.
8.
2012

Albee Messing; Rong Li; Sakkubai Naidu; J Paul Taylor; Lital Silverman; Daniel Flint; Marjo S van der Knaap; Michael Brenner

Archetypal and new families with Alexander disease and novel mutations in GFAP.
Archives of neurology 2012;69(2):208-14.
9.
2012

Parastoo Jangouk; Kathleen M Zackowski; Sakkubai Naidu; Gerald V Raymond

Adrenoleukodystrophy in female heterozygotes: underrecognized and undertreated.
Molecular genetics and metabolism 2012;105(2):180-5.
10.
2011

Mary E Blue; Walter E Kaufmann; Joseph Bressler; Charlotte Eyring; Cliona O'driscoll; Sakkubai Naidu; Michael V Johnston

Temporal and regional alterations in NMDA receptor expression in Mecp2-null mice.
Anatomical record (Hoboken, N.J. : 2007) 2011;294(10):1624-34.
11.
2011

Ying Wang; Rachel Busin; Catherine Reeves; Lena Bezman; Gerald Raymond; Cicely J Toomer; Paul A Watkins; Ann Snowden; Ann Moser; Sakkubai Naidu; et al.

X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism.
Molecular genetics and metabolism 2011;104(1-2):160-6.
12.
2011

Sakkubai Naidu; Michael V Johnston

Neurodevelopmental disorders: Clinical criteria for Rett syndrome.
Nature reviews. Neurology 2011;7(6):312-4.
13.
2010

Jay R Shapiro; Genila Bibat; Girish Hiremath; Mary E Blue; Shilpa Hundalani; Theodore Yablonski; Aditi Kantipuly; Charles Rohde; Michael Johnston; Sakkubai Naidu

Bone mass in Rett syndrome: association with clinical parameters and MECP2 mutations.
Pediatric research 2010;68(5):446-51.
14.
2010

Deepali Jain; Kamaljeet Singh; Sankar Chirumamilla; Genila M Bibat; Mary E Blue; Sakkubai R Naidu; Charles G Eberhart

Ocular MECP2 protein expression in patients with and without Rett syndrome.
Pediatric neurology 2010;43(1):35-40.
15.
2010

Joseph P Pillion; Genila Bibat; Sakkubai Naidu

Effects of sedation on auditory brainstem response in Rett syndrome.
Pediatric neurology 2010;42(5):331-4.
16.
2010

A Mahmood; G Bibat; A-L Zhan; I Izbudak; L Farage; A Horska; S Mori; S Naidu

White matter impairment in Rett syndrome: diffusion tensor imaging study with clinical correlations.
AJNR. American journal of neuroradiology 2010;31(2):295-9.
17.
2010

Garilyn M Jentarra; Shannon L Olfers; Stephen G Rice; Nishit Srivastava; Gregg E Homanics; Mary Blue; Sakkubai Naidu; Vinodh Narayanan

Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation.
BMC neuroscience 2010;11():19.
18.
2009

Maria Teresa Dotti; Rosaria Buccoliero; Andrew Lee; J Raphael Gorospe; Daniel Flint; Paolo Galluzzi; Silvia Bianchi; Camilla D'Eramo; Sakkubai Naidu; Antonio Federico; et al.

An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variant.
Journal of neurology 2009;256(4):679-82.
19.
2009

Z Yapici; G Benbir; S Saltik; L He; G K Brown; R W Taylor; A Dincer; S Naidu; C Yalcinkaya

Two cases with progressive cystic leukoencephalopathy.
Neuropediatrics 2009;40(1):47-51.
20.
2009

Alena Horská; Luciano Farage; Genila Bibat; Lídia M Nagae; Walter E Kaufmann; Peter B Barker; SakkuBai Naidu

Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.
Annals of neurology 2009;65(1):90-7.
21.
2008

J C Carter; D C Lanham; D Pham; G Bibat; S Naidu; W E Kaufmann

Selective cerebral volume reduction in Rett syndrome: a multiple-approach MR imaging study.
AJNR. American journal of neuroradiology 2008;29(3):436-41.
22.
2007

J C Russell; M E Blue; M V Johnston; S Naidu; M A Hossain

Enhanced cell death in MeCP2 null cerebellar granule neurons exposed to excitotoxicity and hypoxia.
Neuroscience 2007;150(3):563-74.
23.
2006

Grace M Hobson; Zhong Huang; Karen Sperle; Erik Sistermans; Peter K Rogan; James Y Garbern; Edwin Kolodny; Sakkubai Naidu; Franca Cambi

Splice-site contribution in alternative splicing of PLP1 and DM20: molecular studies in oligodendrocytes.
Human mutation 2006;27(1):69-77.
24.
2005

SakkuBai Naidu; Genila Bibat; Doris Lin; Peter Burger; Peter Barker; Sergio Rosemberg; Nancy Braverman; Hugo Arroyo; Michael Dowling; Ada Hamosh; et al.

Progressive cavitating leukoencephalopathy: a novel childhood disease.
Annals of neurology 2005;58(6):929-38.
25.
2005

Michael V Johnston; Mary E Blue; Sakkubai Naidu

Rett syndrome and neuronal development.
Journal of child neurology 2005;20(9):759-63.
26.
2005

Walter E Kaufmann; Mohammed H Jarrar; Judy S Wang; Ye-Jin M Lee; Sriram Reddy; Genila Bibat; Sakkubai Naidu

Histone modifications in Rett syndrome lymphocytes: a preliminary evaluation.
Brain & development 2005;27(5):331-9.
27.
2005

M Henneke; N Preuss; V Engelbrecht; F Aksu; E Bertini; G Bibat; K Brockmann; C Hübner; M Mayer; V Mejaski-Bosnjak; et al.

Cystic leukoencephalopathy without megalencephaly: a distinct disease entity in 15 children.
Neurology 2005;64(8):1411-6.
28.
2005

S A Yatsenko; S W Cheung; D A Scott; M J M Nowaczyk; M Tarnopolsky; S Naidu; G Bibat; A Patel; J G Leroy; F Scaglia; et al.

Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly.
Journal of medical genetics 2005;42(4):328-35.
29.
2005

Rong Li; Anne B Johnson; Gajja Salomons; James E Goldman; Sakkubai Naidu; Roy Quinlan; Bruce Cree; Stephanie Z Ruyle; Brenda Banwell; Marc D'Hooghe; et al.

Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease.
Annals of neurology 2005;57(3):310-26.
30.
2004

L M Nagae-Poetscher; G Bibat; M Philippart; S Rosemberg; A Fatemi; M T C Lacerda; M O R Costa; F Kok; C Costa Leite; A Horská; et al.

Leukoencephalopathy, cerebral calcifications, and cysts: new observations.
Neurology 2004;62(7):1206-9.
31.
2004

J R Gorospe; B S Singhal; T Kainu; F Wu; D Stephan; J Trent; E P Hoffman; S Naidu

Indian Agarwal megalencephalic leukodystrophy with cysts is caused by a common MLC1 mutation.
Neurology 2004;62(6):878-82.
32.
2003

Marjo S van der Knaap; Carola G M van Berkel; Jochen Herms; Rudy van Coster; Martina Baethmann; Sakkubai Naidu; Eugen Boltshauser; Michèl A A P Willemsen; Barbara Plecko; Georg F Hoffmann; et al.

eIF2B-related disorders: antenatal onset and involvement of multiple organs.
American journal of human genetics 2003;73(5):1199-207.
33.
2003

SakkuBai Naidu

Rett syndrome: from discovery to current interest.
Journal of child neurology 2003;18(10):661.
34.
2003

SakkuBai Naidu; Genila Bibat; Lisa Kratz; Richard I Kelley; Jonathan Pevsner; Eric Hoffman; Carmen Cuffari; Charles Rohde; Mary E Blue; Michael V Johnston

Clinical variability in Rett syndrome.
Journal of child neurology 2003;18(10):662-8.
35.
2003

Bernard L Maria; Kathleen McCann Deidrick; Hugo Moser; Sakkubai Naidu

Leukodystrophies: pathogenesis, diagnosis, strategies, therapies, and future research directions.
Journal of child neurology 2003;18(9):578-90.
36.
2003

Bhim S Singhal; J Rafael Gorospe; Sakkubai Naidu

Megalencephalic leukoencephalopathy with subcortical cysts.
Journal of child neurology 2003;18(9):646-52.
37.
2003

Francesca Pizzini; Ali S Fatemi; Peter B Barker; Lidia M Nagae-Poetscher; Alena Horská; Andrew W Zimmerman; Hugo W Moser; Genila Bibat; Sakkubai Naidu

Proton MR spectroscopic imaging in Pelizaeus-Merzbacher disease.
AJNR. American journal of neuroradiology 2003;24(8):1683-9.
38.
2003

Gabriele V Ronnett; Donald Leopold; Xiaohe Cai; Kristen C Hoffbuhr; Linda Moses; Eric P Hoffman; Sakkubai Naidu

Olfactory biopsies demonstrate a defect in neuronal development in Rett's syndrome.
Annals of neurology 2003;54(2):206-18.
39.
2003

Joseph P Pillion; Vishakha W Rawool; Genila Bibat; Sakkubai Naidu

Prevalence of hearing loss in Rett syndrome.
Developmental medicine and child neurology 2003;45(5):338-43.
40.
2003

A Fatemi; P B Barker; A M Uluğ; L M Nagae-Poetscher; N J Beauchamp; A B Moser; G V Raymond; H W Moser; S Naidu

MRI and proton MRSI in women heterozygous for X-linked adrenoleukodystrophy.
Neurology 2003;60(8):1301-7.
41.
2002

Marjo S van der Knaap; SakkuBai Naidu; Petra J W Pouwels; Simona Bonavita; Rudy van Coster; Lieven Lagae; Jürgen Sperner; Robert Surtees; Raphael Schiffmann; Jakob Valk

New syndrome characterized by hypomyelination with atrophy of the basal ganglia and cerebellum.
AJNR. American journal of neuroradiology 2002;23(9):1466-74.
42.
2002

Patricia M Villemagne; Sakkubai Naidu; Victor L Villemagne; Myron Yaster; Henry N Wagner; James C Harris; Hugo W Moser; Michael V Johnston; Robert F Dannals; Dean F Wong

Brain glucose metabolism in Rett Syndrome.
Pediatric neurology 2002;27(2):117-22.
43.
2002

J R Gorospe; S Naidu; A B Johnson; V Puri; G V Raymond; S D Jenkins; R C Pedersen; D Lewis; P Knowles; R Fernandez; et al.

Molecular findings in symptomatic and pre-symptomatic Alexander disease patients.
Neurology 2002;58(10):1494-500.
44.
2002

Marjo S van der Knaap; Peter A J Leegwater; Andrea A M Könst; Allerdien Visser; Sakkubai Naidu; Cees B M Oudejans; Ruud B H Schutgens; Jan C Pronk

Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter.
Annals of neurology 2002;51(2):264-70.
45.
2002

Alena Horská; Walter E Kaufmann; Larry J Brant; Sakkubai Naidu; James C Harris; Peter B Barker

In vivo quantitative proton MRSI study of brain development from childhood to adolescence.
Journal of magnetic resonance imaging : JMRI 2002;15(2):137-43.
46.
2002

K C Hoffbuhr; L M Moses; M A Jerdonek; S Naidu; E P Hoffman

Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.
Mental retardation and developmental disabilities research reviews 2002;8(2):99-105.
47.
2001

P A Leegwater; G Vermeulen; A A Könst; S Naidu; J Mulders; A Visser; P Kersbergen; D Mobach; D Fonds; C G van Berkel; et al.

Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter.
Nature genetics 2001;29(4):383-8.
48.
2001

S Naidu; W E Kaufmann; M T Abrams; G D Pearlson; D C Lanham; K A Fredericksen; P B Barker; A Horska; X Golay; S Mori; et al.

Neuroimaging studies in Rett syndrome.
Brain & development 2001;23 Suppl 1():S62-71.
49.
2001

M V Johnston; O H Jeon; J Pevsner; M E Blue; S Naidu

Neurobiology of Rett syndrome: a genetic disorder of synapse development.
Brain & development 2001;23 Suppl 1():S206-13.
50.
2001

C Colantuoni; O H Jeon; K Hyder; A Chenchik; A H Khimani; V Narayanan; E P Hoffman; W E Kaufmann; S Naidu; J Pevsner

Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification.
Neurobiology of disease 2001;8(5):847-65.
51.
2001

A M Kerr; Y Nomura; D Armstrong; M Anvret; P V Belichenko; S Budden; H Cass; J Christodoulou; A Clarke; C Ellaway; et al.

Guidelines for reporting clinical features in cases with MECP2 mutations.
Brain & development 2001;23(4):208-11.
52.
2001

K Hoffbuhr; J M Devaney; B LaFleur; N Sirianni; C Scacheri; J Giron; J Schuette; J Innis; M Marino; M Philippart; et al.

MeCP2 mutations in children with and without the phenotype of Rett syndrome.
Neurology 2001;56(11):1486-95.
53.
2001

H S Singer; S Naidu

Rett syndrome: "We'll keep the genes on for you".
Neurology 2001;56(5):582-4.
54.
2001

M S van der Knaap; S Naidu; S N Breiter; S Blaser; H Stroink; S Springer; J C Begeer; R van Coster; P G Barth; N H Thomas; et al.

Alexander disease: diagnosis with MR imaging.
AJNR. American journal of neuroradiology 2001;22(3):541-52.
55.
2000

J P Pillion; S Naidu

Auditory brainstem response findings in Rett syndrome: stability over time.
The Journal of pediatrics 2000;137(3):393-6.
56.
2000

L Farina; A Bizzi; G Finocchiaro; D Pareyson; A Sghirlanzoni; B Bertagnolio; M Savoiardo; S Naidu; B S Singhal; D A Wenger

MR imaging and proton MR spectroscopy in adult Krabbe disease.
AJNR. American journal of neuroradiology 2000;21(8):1478-82.
57.
2000

J P Pillion; V W Rawool; S Naidu

Auditory brainstem responses in Rett syndrome: effects of hyperventilation, seizures, and tympanometric variables.
Audiology : official organ of the International Society of Audiology 2000;39(2):80-7.
58.
2000

A Horská; S Naidu; E H Herskovits; P Y Wang; W E Kaufmann; P B Barker

Quantitative 1H MR spectroscopic imaging in early Rett syndrome.
Neurology 2000;54(3):715-22.
59.
2000

M S van der Knaap; S Naidu; B K Kleinschmidt-Demasters; W Kamphorst; H C Weinstein

Autosomal dominant diffuse leukoencephalopathy with neuroaxonal spheroids.
Neurology 2000;54(2):463-8.
60.
1999

M Wan; S S Lee; X Zhang; I Houwink-Manville; H R Song; R E Amir; S Budden; S Naidu; J L Pereira; I F Lo; et al.

Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots.
American journal of human genetics 1999;65(6):1520-9.
61.
1999

M S van der Knaap; S N Breiter; S Naidu; A A Hart; J Valk

Defining and categorizing leukoencephalopathies of unknown origin: MR imaging approach.
Radiology 1999;213(1):121-33.
62.
1999

P A Leegwater; A A Könst; B Kuyt; L A Sandkuijl; S Naidu; C B Oudejans; R B Schutgens; J C Pronk; M S van der Knaap

The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27.
American journal of human genetics 1999;65(3):728-34.
63.
1999

W R Kates; I S Warsofsky; A Patwardhan; M T Abrams; A M Liu; S Naidu; W E Kaufmann; A L Reiss

Automated Talairach atlas-based parcellation and measurement of cerebral lobes in children.
Psychiatry research 1999;91(1):11-30.
64.
1999

M E Blue; S Naidu; M V Johnston

Development of amino acid receptors in frontal cortex from girls with Rett syndrome.
Annals of neurology 1999;45(4):541-5.
65.
1999

M E Blue; S Naidu; M V Johnston

Altered development of glutamate and GABA receptors in the basal ganglia of girls with Rett syndrome.
Experimental neurology 1999;156(2):345-52.
66.
1999

M E Hodes; A W Zimmerman; A Aydanian; S Naidu; N R Miller; J L Garcia Oller; B Barker; K A Aleck; T D Hurley; S R Dlouhy

Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2).
American journal of medical genetics 1999;82(2):132-9.
67.
1999

A B Moser; N Kreiter; L Bezman; S Lu; G V Raymond; S Naidu; H W Moser

Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls.
Annals of neurology 1999;45(1):100-10.
68.
1998

N Sirianni; S Naidu; J Pereira; R F Pillotto; E P Hoffman

Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28.
American journal of human genetics 1998;63(5):1552-8.
69.
1998

V Narayanan; S Olinsky; E Dahle; S Naidu; H Y Zoghbi

Mutation analysis of the M6b gene in patients with Rett syndrome.
American journal of medical genetics 1998;78(2):165-8.
70.
1998

E Niedermeyer; S B Naidu

Rett syndrome, EEG and the motor cortex as a model for better understanding of attention deficit hyperactivity disorder (ADHD).
European child & adolescent psychiatry 1998;7(2):69-72.
71.
1998

D F Wong; G Ricaurte; G Gründer; R Rothman; S Naidu; H Singer; J Harris; F Yokoi; V Villemagne; S Szymanski; et al.

Dopamine transporter changes in neuropsychiatric disorders.
Advances in pharmacology (San Diego, Calif.) 1998;42():219-23.
72.
1997

S Naidu; S R Dlouhy; M T Geraghty; M E Hodes

A male child with the rumpshaker mutation, X-linked spastic paraplegia/Pelizaeus-Merzbacher disease and lysinuria.
Journal of inherited metabolic disease 1997;20(6):811-6.
73.
1997

S B Naidu

Rett syndrome.
Indian journal of pediatrics 1997;64(5):651-9.
74.
1997

A H Hoon; E M Reinhardt; R I Kelley; S N Breiter; D H Morton; S B Naidu; M V Johnston

Brain magnetic resonance imaging in suspected extrapyramidal cerebral palsy: observations in distinguishing genetic-metabolic from acquired causes.
The Journal of pediatrics 1997;131(2):240-5.
75.
1997

S Naidu

Rett syndrome: a disorder affecting early brain growth.
Annals of neurology 1997;42(1):3-10.
76.
1997

E Niedermeyer; S B Naidu

Attention-deficit hyperactivity disorder (ADHD) and frontal-motor cortex disconnection.
Clinical EEG (electroencephalography) 1997;28(3):130-6.
77.
1997

S S el-Deiry; S Naidu; L S Blevins; P W Ladenson

Assessment of adrenal function in women heterozygous for adrenoleukodystrophy.
The Journal of clinical endocrinology and metabolism 1997;82(3):856-60.
78.
1997

B Subramaniam; S Naidu; A L Reiss

Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa.
Neurology 1997;48(2):399-407.
79.
1997

E Niedermeyer; S B Naidu; C Plate

Unusual EEG theta rhythms over central region in Rett syndrome: considerations of the underlying dysfunction.
Clinical EEG (electroencephalography) 1997;28(1):36-43.
80.
1997

S Naidu

Rett syndrome: natural history and underlying disease mechanisms.
European child & adolescent psychiatry 1997;6 Suppl 1():14-7.
81.
1997

W E Kaufmann; C V Taylor; C F Hohmann; I B Sanwal; S Naidu

Abnormalities in neuronal maturation in Rett syndrome neocortex: preliminary molecular correlates.
European child & adolescent psychiatry 1997;6 Suppl 1():75-7.
82.
1996

D Edwin; L J Speedie; W Kohler; S Naidu; B Kruse; H W Moser

Cognitive and brain magnetic resonance imaging findings in adrenomyeloneuropathy.
Annals of neurology 1996;40(4):675-8.
83.
1996

D F Wong; J C Harris; S Naidu; F Yokoi; S Marenco; R F Dannals; H T Ravert; M Yaster; A Evans; O Rousset; et al.

Dopamine transporters are markedly reduced in Lesch-Nyhan disease in vivo.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(11):5539-43.
84.
1996

W E Kaufmann; C Theda; S Naidu; P A Watkins; A B Moser; H W Moser

Neuronal migration abnormality in peroxisomal bifunctional enzyme defect.
Annals of neurology 1996;39(2):268-71.
85.
1995

A B Moser; M Rasmussen; S Naidu; P A Watkins; M McGuinness; A K Hajra; G Chen; G Raymond; A Liu; D Gordon

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups.
The Journal of pediatrics 1995;127(1):13-22.
86.
1995

S Hosain; W E Kaufmann; G Negrin; P A Watkins; A N Siakotos; D N Palmer; S Naidu

Diagnoses of neuronal ceroid-lipofuscinosis by immunochemical methods.
American journal of medical genetics 1995;57(2):239-45.
87.
1995

A J Kumar; W Köhler; B Kruse; S Naidu; A Bergin; D Edwin; H W Moser

MR findings in adult-onset adrenoleukodystrophy.
AJNR. American journal of neuroradiology 1995;16(6):1227-37.
88.
1995

W E Kaufmann; S Naidu; S Budden

Abnormal expression of microtubule-associated protein 2 (MAP-2) in neocortex in Rett syndrome.
Neuropediatrics 1995;26(2):109-13.
89.
1995

S Naidu; S Hyman; E L Harris; V Narayanan; D Johns; F Castora

Rett syndrome studies of natural history and search for a genetic marker.
Neuropediatrics 1995;26(2):63-6.
90.
1995

B R Migeon; M A Dunn; G Thomas; B J Schmeckpeper; S Naidu

Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome.
American journal of human genetics 1995;56(3):647-53.
91.
1995

V M Pratt; S Naidu; S R Dlouhy; H G Marks; M E Hodes

A novel mutation in exon 3 of the proteolipid protein gene in Pelizaeus-Merzbacher disease.
Neurology 1995;45(2):394-5.
92.
1995

D W Cooke; S Naidu; L Plotnick; G D Berkovitz

Abnormalities of thyroid function and glucose control in subjects with Rett syndrome.
Hormone research 1995;43(6):273-8.
93.
1994

S Naidu; H W Moser

Peroxisomal disorders.
Neurologic clinics 1994;12(4):727-39.
94.
1994

T Itoh; S Magnaldi; R M White; M B Denckla; K Hofman; S Naidu; R N Bryan

Neurofibromatosis type 1: the evolution of deep gray and white matter MR abnormalities.
AJNR. American journal of neuroradiology 1994;15(8):1513-9.
95.
1994

C L Marcus; J L Carroll; S A McColley; G M Loughlin; S Curtis; P Pyzik; S Naidu

Polysomnographic characteristics of patients with Rett syndrome.
The Journal of pediatrics 1994;125(2):218-24.
96.
1994

C J Danpure; P Fryer; S Griffiths; K M Guttridge; P R Jennings; J Allsop; A B Moser; S Naidu; H W Moser; M MacCollin

Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism.
Journal of inherited metabolic disease 1994;17(1):27-40.
97.
1993

A L Reiss; F Faruque; S Naidu; M Abrams; T Beaty; R N Bryan; H Moser

Neuroanatomy of Rett syndrome: a volumetric imaging study.
Annals of neurology 1993;34(2):227-34.
98.
1993

G L Wenk; M O'Leary; C B Nemeroff; G Bissette; H Moser; S Naidu

Neurochemical alterations in Rett syndrome.
Brain research. Developmental brain research 1993;74(1):67-72.
99.
1993

C Theda; R C Woody; S Naidu; A B Moser; H W Moser

Increased very long chain fatty acids in patients on a ketogenic diet: a cause of diagnostic confusion.
The Journal of pediatrics 1993;122(5 Pt 1):724-6.
100.
1993

I U Scott; W R Green; A K Goyal; Z de la Cruz; S Naidu; H Moser

New sites of ocular involvement in late-infantile metachromatic leukodystrophy revealed by histopathologic studies.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 1993;231(3):187-91.
101.
1993

S Naidu

Movement disorders in neuronal ceroid-lipofuscinoses.
Journal of inherited metabolic disease 1993;16(2):256-8.
102.
1992

P B Barker; R N Bryan; A J Kumar; S Naidu

Proton NMR spectroscopy of Canavan's disease.
Neuropediatrics 1992;23(5):263-7.
103.
1992

B Hagberg; S Naidu; A K Percy

Tokyo symposium on the Rett syndrome: neurobiological approach--concluding remarks and epilogue.
Brain & development 1992;14 Suppl():S151-3.
104.
1992

S Naidu; D F Wong; C Kitt; G Wenk; H W Moser

Positron emission tomography in the Rett syndrome: clinical, biochemical and pathological correlates.
Brain & development 1992;14 Suppl():S75-9.
105.
1991

G L Wenk; S Naidu; M F Casanova; C A Kitt; H Moser

Altered neurochemical markers in Rett's syndrome.
Neurology 1991;41(11):1753-6.
106.
1991

S Naidu; H Moser

Infantile Refsum disease.
AJNR. American journal of neuroradiology 1991;12(6):1161-3.
107.
1991

H W Moser; A Bergin; S Naidu; P W Ladenson

Adrenoleukodystrophy.
Endocrinology and metabolism clinics of North America 1991;20(2):297-318.
108.
1991

S Naidu; H W Moser

Value of neuroimaging in metabolic diseases affecting the CNS.
AJNR. American journal of neuroradiology 1991;12(3):413-6.
109.
1991

H W Moser; A B Moser; S Naidu; A Bergin

Clinical aspects of adrenoleukodystrophy and adrenomyeloneuropathy.
Developmental neuroscience 1991;13(4-5):254-61.
110.
1991

M F Casanova; S Naidu; T E Goldberg; H W Moser; S Khoromi; A Kumar; J E Kleinman; D R Weinberger

Quantitative magnetic resonance imaging in Rett syndrome.
The Journal of neuropsychiatry and clinical neurosciences 1991;3(1):66-72.
111.
1990

S Naidu; H W Moser

Peroxisomal disorders.
Neurologic clinics 1990;8(3):507-28.
112.
1990

E M Goldstein; S Naidu

Degenerative disorders of the brain--a clinical and biochemical approach.
Indian journal of pediatrics 1990;57(4):499-516.
113.
1990

D Edwin; L Speedie; S Naidu; H Moser

Cognitive impairment in adult-onset adrenoleukodystrophy.
Molecular and chemical neuropathology / sponsored by the International Society for Neurochemistry and the World Federation of Neurology and research groups on neurochemistry and cerebrospinal fluid 1990;12(3):167-76.
114.
1990

R J Tusa; P W Kaplan; T C Hain; S Naidu

Ipsiversive eye deviation and epileptic nystagmus.
Neurology 1990;40(4):662-5.
115.
1990

S Naidu; S Hyman; K Piazza; J Savedra; J Perman; G Wenk; C Kitt; J Troncoso; D Price; M Cassanova

The Rett syndrome: progress report on studies at the Kennedy Institute.
Brain & development 1990;12(1):5-7.
116.
1990

E Niedermeyer; S Naidu

Further EEG observations in children with the Rett syndrome.
Brain & development 1990;12(1):53-4.
117.
1989

S Naidu; K Rajyalakshmi; A S Naidu

Risk involvement with Staphylococcus aureus exotoxins among pyogenic skin infections with special reference to toxic shock syndrome.
Acta microbiologica Hungarica 1989;36(1):7-12.
118.
1988

S Naidu; M J Bresnan; D Griffin; S O'Toole; H W Moser

Childhood adrenoleukodystrophy. Failure of intensive immunosuppression to arrest neurologic progression.
Archives of neurology 1988;45(8):846-8.
119.
1988

S Naidu; G Hoefler; P A Watkins; W W Chen; A B Moser; S Hoefler; N E Rance; J M Powers; M Beard; W R Green

Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entity.
Neurology 1988;38(7):1100-7.
120.
1988

H Shimizu; H W Moser; S Naidu

Auditory brainstem response and audiologic findings in adrenoleukodystrophy: its variant and carrier.
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 1988;98(3):215-20.
121.
1988

S Naidu; K J Hofmann; H W Moser; I H Maumenee; D A Wenger

Galactosylceramide-beta-galactosidase deficiency in association with cherry red spot.
Neuropediatrics 1988;19(1):46-8.
122.
1988

S Naidu; I Maumanee; J Olson; J Borel; H Moser

Selenium treatment in neuronal ceroid-lipofuscinosis.
American journal of medical genetics. Supplement 1988;5():283-9.
123.
1988

A K Percy; R H Haas; E Kolodny; H Moser; S Naidu

Recommendations regarding handling of the necropsy in Rett syndrome.
Journal of child neurology 1988;3 Suppl():S91-3.
124.
1988

D F Wong; E P Broussolle; G Wand; V Villemagne; R F Dannals; J M Links; H A Zacur; J Harris; S Naidu; C Braestrup

In vivo measurement of dopamine receptors in human brain by positron emission tomography. Age and sex differences.
Annals of the New York Academy of Sciences 1988;515():203-14.
125.
1988

E Trevathan; S Naidu

The clinical recognition and differential diagnosis of Rett syndrome.
Journal of child neurology 1988;3 Suppl():S6-16.
126.
1988

S Naidu; C A Kitt; D F Wong; D L Price; J C Troncoso; H W Moser

Research on Rett syndrome: strategy and preliminary results.
Journal of child neurology 1988;3 Suppl():S78-86.
127.
1988

S Naidu; A E Moser; H W Moser

Phenotypic and genotypic variability of generalized peroxisomal disorders.
Pediatric neurology 1988;4(1):5-12.
128.
1987

A J Kumar; A E Rosenbaum; S Naidu; L Wener; C M Citrin; R Lindenberg; W S Kim; S J Zinreich; M E Molliver; H S Mayberg

Adrenoleukodystrophy: correlating MR imaging with CT.
Radiology 1987;165(2):497-504.
129.
1987

A B Moser; J Borel; A Odone; S Naidu; D Cornblath; D B Sanders; H W Moser

A new dietary therapy for adrenoleukodystrophy: biochemical and preliminary clinical results in 36 patients.
Annals of neurology 1987;21(3):240-9.
130.
1987

S Naidu; S Chatterjee; M Murphy; S Uematsu; M Phillapart; H Moser

Rett syndrome: new observations.
Brain & development 1987;9(5):525-8.
131.
1987

P A Watkins; S Naidu; H W Moser

Adrenoleukodystrophy: biochemical procedures in diagnosis, prevention and treatment.
Journal of inherited metabolic disease 1987;10 Suppl 1():46-53.
132.
1987

K J Hofman; S Naidu; H W Moser; I H Maumenee; D A Wenger

Cherry red spot in association with galactosylceramide-beta-galactosidase deficiency.
Journal of inherited metabolic disease 1987;10(3):273-4.
133.
1987

M Coleman; S Naidu; M Murphy; M Pines; W Bias

A set of monozygotic twins with Rett syndrome.
Brain & development 1987;9(5):475-8.
134.
1987

H W Moser; S Naidu; A J Kumar; A E Rosenbaum

The adrenoleukodystrophies.
Critical reviews in neurobiology 1987;3(1):29-88.
135.
1986

S Naidu; G Gruener; P Brazis

Excellent results with clorazepate in recalcitrant childhood epilepsies.
Pediatric neurology 1986;2(1):18-22.
136.
1986

E Niedermeyer; A Rett; H Renner; M Murphy; S Naidu

Rett syndrome and the electroencephalogram.
American journal of medical genetics. Supplement 1986;1():195-9.
137.
1986

J C Harris; D F Wong; H N Wagner; A Rett; S Naidu; R F Dannals; J M Links; M L Batshaw; H W Moser

Positron emission tomographic study of D2 dopamine receptor binding and CSF biogenic amine metabolites in Rett syndrome.
American journal of medical genetics. Supplement 1986;1():201-10.
138.
1986

J W Moore; C M Tuck-Muller; M Murphy; S Naidu; G H Thomas

Chromosome studies in 10 patients with the Rett syndrome.
American journal of medical genetics. Supplement 1986;1():345-54.
139.
1986

S Naidu; M Murphy; H W Moser; A Rett

Rett syndrome--natural history in 70 cases.
American journal of medical genetics. Supplement 1986;1():61-72.
140.
1986

M Murphy; S Naidu; H W Moser

Rett syndrome--observational study of 33 families.
American journal of medical genetics. Supplement 1986;1():73-6.
141.
1983

M H Naheedy; S Naidu; A J Griffin

Prolonged retention of contrast medium in an hypoxic neonatal brain.
Surgical neurology 1983;20(5):369-72.
142.
1983

S Naidu; H Messmore; V Caserta; M Fine

CNS lesions in neonatal isoimmune thrombocytopenia.
Archives of neurology 1983;40(9):552-4.
143.
1983

R Matalon; S Naidu; J R Hughes; K Michals

Nonketotic hyperglycinemia: treatment with diazepam--a competitor for glycine receptors.
Pediatrics 1983;71(4):581-4.
144.
1982

J C Masdeu; M Fine; D A Shewmon; E Palacios; S Naidu

Postischemic hypervascularity of the infant brain: differential diagnosis on computed tomography.
AJNR. American journal of neuroradiology 1982;3(5):501-4.
145.
1982

S Naidu; G Glista; M Fine; J Brumlik; E Palacios

Serial CT scans in Haemophilus influenzae meningitis of childhood.
Developmental medicine and child neurology 1982;24(1):69-76.
146.
1981

M J Danon; S J Oh; S DiMauro; J R Manaligod; A Eastwood; S Naidu; L H Schliselfeld

Lysosomal glycogen storage disease with normal acid maltase.
Neurology 1981;31(1):51-7.
147.
1980

S Naidu; N Narasimhachari

Sydenham's chorea: a possible presynaptic dopaminergic dysfunction initially.
Annals of neurology 1980;8(4):445-7.
148.
1978

S Naidu; L I Wolfson; N S Sharpless

Juvenile parkinsonism: a patient with possible primary striatal dysfunction.
Annals of neurology 1978;3(5):453-5.

Sakkubai Naidu The Johns Hopkins Medical Institutions, Kennedy Krieger Institute

Sakkubai Naidu

148 Publications

Sakkubai Naidu
The Johns Hopkins Medical Institutions, Kennedy Krieger Institute