Detalhe da pesquisa
1.
Comprehensive immunoprofiling of neurodevelopmental disorders suggests three distinct classes based on increased neurogenesis, Th-1 polarization or IL-1 signaling.
Brain Behav Immun
; 115: 505-516, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37972879
2.
Genotype-phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India.
Neurogenetics
; 24(1): 43-53, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36580222
3.
Altered cerebellar lobular volumes correlate with clinical deficits in siblings and children with ASD: evidence from toddlers.
J Transl Med
; 21(1): 246, 2023 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37029372
4.
Systemic inflammatory syndrome in COVID-19-SISCoV study: systematic review and meta-analysis.
Pediatr Res
; 91(6): 1334-1349, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34006982
5.
Disorders of Tetrahydrobiopterin Metabolism: Experience from South India.
Metab Brain Dis
; 37(3): 743-760, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34997870
6.
Pediatric neurobrucellosis: a systematic review with case report.
J Trop Pediatr
; 69(1)2022 12 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36708042
7.
Macula as a Window to Diagnosis.
J Pediatr
; 231: 284-285, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33333116
8.
Reversible leukoencephalopathy and cerebral atrophy in homocystinuria due to MTHFR deficiency: A treatable metabolic disorder.
J Inherit Metab Dis
; 44(6): 1505-1506, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34541688
9.
Episodic hemiparesis precipitated by trauma.
Childs Nerv Syst
; 36(3): 455-456, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31938869
10.
'All that waddles is not dystrophy'.
J Paediatr Child Health
; 56(2): 339-340, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32045122
11.
Bilateral Posterior Circulation Stroke in a Child with Type 1 Diabetes Mellitus.
Neuropediatrics
; 50(1): 64-65, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30453356
12.
Stiffness, Facial Dysmorphism, and Skeletal Abnormalities: Schwartz-Jampel Syndrome 1A.
J Pediatr
; 200: 286-286.e1, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29866592
13.
Parental KAP and its Relation with the Quality of Life in Children with Epilepsy.
Ann Indian Acad Neurol
; 26(4): 419-423, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37970311
14.
Phenotypic features of epilepsy due to sodium channelopathies - A single center experience from India.
J Neurosci Rural Pract
; 14(4): 603-609, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38059254
15.
Collagen XII-Related Myopathy: An Emerging Spectrum of Extracellular Matrix-Related Myopathy.
Neurol India
; 71(6): 1257-1259, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38174471
16.
MYH2-related Myopathy: Expanding the Clinical Spectrum of Chronic Progressive External Ophthalmoplegia (CPEO).
J Neuromuscul Dis
; 10(4): 727-730, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37154181
17.
Clinical, imaging and genetic profile of twenty-four patients with pantothenate kinase-associated neurodegeneration (PKAN)- A single centre study from India.
Parkinsonism Relat Disord
; 111: 105409, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37121191
18.
Hereditary Sensory and Autonomic Neuropathy: A Case Series of Six Children.
Neurol India
; 70(1): 231-237, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35263888
19.
Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children.
Mov Disord Clin Pract
; 9(7): 886-899, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36247901
20.
DNAJC6 mutation causing cranial-onset dystonia with tremor dominant levodopa non-responsive parkinsonism: A novel phenotype.
Parkinsonism Relat Disord
; 89: 1-3, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34175496