دنبال کردن
Inusha Panigrahi
Inusha Panigrahi
ایمیل تأیید شده در pgimer.edu.in - صفحهٔ اصلی
عنوان
نقل شده توسط
نقل شده توسط
سال
The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery.
CYJ Toriyama M, Lee C, Taylor SP, Duran I, Cohn DH, Bruel AL, Tabler JM ...
Nature Genetics, 2016
1622016
Fifteen years of research on oral–facial–digital syndromes: from 1 to 16 causal genes
AL Bruel, B Franco, Y Duffourd, J Thevenon, L Jego, E Lopez, JF Deleuze, ...
Journal of medical genetics 54 (6), 371-380, 2017
1212017
Primordial dwarfism: overview of clinical and genetic aspects
P Khetarpal, S Das, I Panigrahi, A Munshi
Molecular Genetics and Genomics 291, 1-15, 2016
782016
The effect of prophylactic antipyretic administration on post-vaccination adverse reactions and antibody response in children: a systematic review
RR Das, I Panigrahi, SS Naik
PLoS One 9 (9), e106629, 2014
772014
Role of MTHFR C677T polymorphism in ischemic stroke
I Panigrahi, T Chatterjee, A Biswas, M Behari, PV Choudhry, R Saxena
Neurology India 54 (1), 48-50, 2006
692006
Craniosynostosis genetics: The mystery unfolds
I Panigrahi
Indian Journal of Human Genetics 17 (2), 48, 2011
652011
Thromboembolic complications in β-thalassemia: beyond the horizon
I Panigrahi, S Agarwal
Thrombosis research 120 (6), 783-789, 2007
652007
Hemoglobin E-beta thalassemia: factors affecting phenotype
I Panigrahi, S Agarwal, T Gupta, P Singhal, M Pradhan
Indian Pediatr 42 (4), 357-362, 2005
562005
Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation
J Sheth, R Bhavsar, M Mistri, D Pancholi, A Bavdekar, A Dalal, ...
BMC medical genetics 20, 1-11, 2019
532019
Response to zolendronic acid in children with type III osteogenesis imperfecta
I Panigrahi, RR Das, S Sharda, RK Marwaha, N Khandelwal
Journal of bone and mineral metabolism 28, 451-455, 2010
522010
Mutational spectrum of thalassemias in India
I Panigrahi, RK Marwaha
Indian journal of human genetics 13 (1), 36, 2007
492007
Rubinstein-Taybi syndrome: Clinical profile of 11 patients and review of literature
S Kumar, R Suthar, I Panigrahi, RK Marwaha
Indian journal of human genetics 18 (2), 161, 2012
482012
Clinical and molecular diagnosis of spinal muscular atrophy
I Panigrahi, A Kesari, SR Phadke, B Mittal
Neurology India 50 (2), 117-122, 2002
482002
Do alpha deletions influence hydroxyurea response in thalassemia intermedia?
I Panigrahi, A Dixit, S Arora, M Kabra, M Mahapatra, VP Choudhry, ...
Hematology 10 (1), 61-63, 2005
422005
Genetic determinants of phenotype in beta-thalassemia
I Panigrahi, S Agarwal
Hematology 13 (4), 247-252, 2008
392008
Chronic lymphocytic leukemia in India-A clinico-hematological profile
N Agrawal, R Naithani, M Mahapatra, I Panigrahi, R Kumar, HP Pati, ...
Hematology 12 (3), 229-233, 2007
392007
Spectrum of anemia in pregnant Indian women and importance of antenatal screening.
M Sinha, I Panigrahi, J Shukla, A Khanna, R Saxena
Indian Journal of Pathology and Microbiology 49 (3), 373-375, 2006
392006
Vitamin D supplementation for the treatment of acute childhood pneumonia: a systematic review
RR Das, M Singh, I Panigrahi, SS Naik
International Scholarly Research Notices 2013 (1), 459160, 2013
382013
Diagnosis of Down syndrome and detection of origin of nondisjunction by short tandem repeat analysis
S Jain, S Agarwal, I Panigrahi, P Tamhankar, S Phadke
Genetic Testing and Molecular Biomarkers 14 (4), 489-491, 2010
322010
CRELD1 gene variants and atrioventricular septal defects in Down syndrome
A Asim, S Agarwal, I Panigrahi, AN Sarangi, S Muthuswamy, A Kapoor
Gene 641, 180-185, 2018
312018
سیستم در حال حاضر قادر به انجام عملکرد نیست. بعداً دوباره امتحان کنید.
مقاله‌ها 1–20