Detalhe da pesquisa
1.
Genomic and computational analysis of four novel variants of MPL gene in Congenital Amegakaryocytic Thrombocytopenia.
Ann Hematol
; 102(10): 2683-2693, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37438490
2.
Novel ANOVA-Statistic-Reduced Deep Fully Connected Neural Network for the Damage Grade Prediction of Post-Earthquake Buildings.
Sensors (Basel)
; 23(14)2023 Jul 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37514735
3.
A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects.
Hum Mutat
; 42(12): 1648-1665, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34585473
4.
Nitric oxide synthase-2 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemia.
Mol Biol Rep
; 48(3): 2519-2525, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33778919
5.
Severe telomere shortening in Fanconi anemia complementation group L.
Mol Biol Rep
; 48(1): 585-593, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33394227
6.
COVID19 in children with cancer in low- and middle-income countries: Experience from a cancer center in Chennai, India.
Pediatr Hematol Oncol
; 38(2): 161-167, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33150828
7.
A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India.
Hum Mutat
; 41(1): 122-128, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31513304
8.
First Counseling Revealing the Diagnosis of Childhood Cancer: Parent Preferences From an Indian Perspective.
J Pediatr Hematol Oncol
; 38(8): 622-626, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27769080
9.
Parent's Perspectives on the End-of-life Care of their Child with Cancer: Indian Perspective.
Indian J Palliat Care
; 22(3): 317-25, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27559262
10.
Acute neurological complications during acute lymphoblastic leukemia therapy: A single-center experience over 10 years.
Indian J Cancer
; 58(4): 545-552, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34380827
11.
Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe haemolytic anaemia with developmental delay in an Indian family.
J Clin Pathol
; 74(10): 620-624, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-33361148
12.
Mitochondrial DNA variations and mitochondrial dysfunction in Fanconi anemia.
PLoS One
; 15(1): e0227603, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31940411
13.
Clinical, Immunological, and Molecular Features of Severe Combined Immune Deficiency: A Multi-Institutional Experience From India.
Front Immunol
; 11: 619146, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33628209
14.
ITP: the dilemma of treatment.
J Pediatr Hematol Oncol
; 36(8): 666, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23799520
15.
Vitamin D insufficiency among children with cancer in India.
Indian J Med Paediatr Oncol
; 37(1): 14-9, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27051151
16.
Co-Incidence or Co-Existence? Acute Lymphoblastic Leukaemia in HbE-alpha Thalassaemia: A Case Report with Review of Literature.
J Clin Diagn Res
; 9(11): XD01-XD02, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26672845
17.
Newly diagnosed immune thrombocytopenia: update on diagnosis and management.
Indian J Pediatr
; 81(10): 1033-41, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24091868
18.
Congenital afibrinogenemia in a new born: a rare cause for bleeding.
Blood Coagul Fibrinolysis
; 25(5): 527-9, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24509333
19.
Severe systemic infection masking underlying childhood leukemia.
Indian J Hematol Blood Transfus
; 29(3): 167-70, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24426366
20.
Tumor lysis syndrome.
Indian J Pediatr
; 80(1): 50-4, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22752730