Detalhe da pesquisa
1.
Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implications.
Clin Genet
; 105(6): 639-654, 2024 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-38374498
2.
Drug Induced Diabetes Mellitus in Pediatric Acute Lymphoblastic Leukemia: Approach to Diagnosis and Management.
J Pediatr Hematol Oncol
; 44(6): 273-279, 2022 08 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35700365
3.
Severe Pulmonary Arterial Hypertension in Healthy Young Infants: Single Center Experience.
Indian Pediatr
; 60(9): 748-751, 2023 09 15.
Artigo
Inglês
| MEDLINE | ID: mdl-37260068
4.
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India.
Eur J Hum Genet
; 2023 Dec 20.
Artigo
Inglês
| MEDLINE | ID: mdl-38114583
5.
Metabolic Bone Disease in Children With Transfusion-Dependent Thalassemia.
Indian Pediatr
; 59(12): 920-923, 2022 12 15.
Artigo
Inglês
| MEDLINE | ID: mdl-36036187
6.
Alopecia Areata and Demyelination as Paraneoplastic Manifestation in Paediatric Hodgkin's Lymphoma.
Int J Hematol Oncol Stem Cell Res
; 12(2): 98-102, 2018 Apr 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30233770
7.
Waldmann's Disease (Primary Intestinal Lymphangiectasia) with Atrial Septal Defect.
J Clin Diagn Res
; 11(4): SD03-SD04, 2017 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-28571224
8.
Super-Refractory Status Epilepticus: A Therapeutic Challenge in Paediatrics.
J Clin Diagn Res
; 11(8): SR01-SR04, 2017 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-28969235
9.
A novel mutation (c.12113T>A) in the polypyrimidine tract of the splice acceptor site of intron 2 causes exon 3 skipping in mitochondrial acetoacetyl-CoA thiolase gene.
Mol Med Rep
; 15(6): 3879-3884, 2017 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-28393214
10.
Guillain-barré syndrome: a clinical study of twenty children.
J Clin Diagn Res
; 9(1): SC09-12, 2015 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-25738052
11.
Merosin-deficient congenital muscular dystrophy with cerebral white matter changes: a clue to its diagnosis beyond infancy.
BMJ Case Rep
; 20142014 Mar 06.
Artigo
Inglês
| MEDLINE | ID: mdl-24604798
12.
Clinicohematological study of thrombocytosis in children.
ISRN Hematol
; 2014: 389257, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-25006474
13.
Purpura fulminans in a child: a case report.
J Clin Diagn Res
; 6(10): 1812-3, 2012 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-23373061
14.
Blue Rubber-Bleb Nevus Syndrome which was Associated with an Atrial Septal Defect: A Case Report.
J Clin Diagn Res
; 6(9): 1566-7, 2012 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-23285461
15.
Ichthyosis congenita with biliary atresia: a rare association.
Clin Dysmorphol
; 26(3): 179-180, 2017 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-27824632
16.
Bilateral type-I duane syndrome with multiple anamolies: a case report.
J Clin Diagn Res
; 6(8): 1435-6, 2012 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-23205369
17.
Avascular Necrosis of Femoral Head in a Child with Beta Thalassaemia Major.
J Clin Diagn Res
; 10(9): SL03, 2016 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-27790543
18.
Disseminated strongyloidiasis in a immunocompromised host.
Indian Pediatr
; 48(12): 974-6, 2011 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-22253157
19.
Hemolytic uremic syndrome associated with Dengue fever in an adolescent girl.
Indian J Pediatr
; 81(12): 1397-8, 2014 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-24623096