Search research articles
Contact Us
Filters
Showing results (121-130 of 159) with videos related to
Page
of 16
Sort By:
Case Reports in Genetics
|
May 30, 2019
Niemann-Pick Disease: An Underdiagnosed Lysosomal Storage Disorder
Inusha Panigrahi, Manoj Dhanorkar, Renu Suthar, et al.
Dermatologic Therapy
|
June 14, 2020
Managing syndromic congenital ichthyosis at a tertiary care institute-Genotype-phenotype correlations, and novel treatments
Garima Dabas, Rahul Mahajan, Dipankar De, et al.
Indian Journal of Pediatrics
|
January 30, 2022
Characterization of the CYP21A2 Gene Mutations in Children with Classic Congenital Adrenal Hyperplasia
Shaily Saraf, Priyanka Srivastava, Inusha Panigrahi, et al.
BMC Pregnancy and Childbirth
|
April 10, 2026
Quantitative proteomic profiling of placental extracellular vesicles in recurrent pregnancy loss reveals their role in feto-maternal crosstalk
Chitra Bhardwaj, Priyanka Srivastava, Ravi Pratap Singh Bhadoriya, et al.
Pediatric Endocrinology, Diabetes, and Metabolism
|
July 19, 2024
Clinical and molecular characterisation of children with monogenic obesity: a case series
Arun George, Santhosh Navi, Pamali Nanda, et al.
Heliyon
|
January 16, 2024
Neurofibromatosis type 1: Clinical characteristics and mutation spectrum in a North Indian cohort
Priyanka Srivastava, Shifali Gupta, Chitra Bamba, et al.
Frontiers in Genetics
|
June 1, 2023
Identification of genetic alterations in couples and their products of conceptions from recurrent pregnancy loss in North Indian population
Priyanka Srivastava, Chitra Bamba, Seema Chopra, et al.
Hematology (Amsterdam, Netherlands)
|
February 28, 2007
Cytochemical, immunophenotypic and ultrastructural characterization of acute leukemias: a prospective study of fifty cases: haematological malignancy
Tathagata Chatterjee, Inusha Panigrahi, Neerja Agrawal, et al.
European Journal of Haematology
|
February 6, 2010
Evaluation of the genetic basis of phenotypic heterogeneity in north Indian patients with thalassemia major
Nidhi Sharma, Reena Das, Jasbir Kaur, et al.
Clinical Dysmorphology
|
March 29, 2019
Phenotypic heterogeneity of kyphoscoliosis with vertebral and rib defects: a case series
Inusha Panigrahi, Suresh Kumar Angurana, Harish Varma, et al.
Page
of 16
Search research articles
Search
Showing results (121-130 of 159) with videos related to
Sort By:
Page
of 16
Case Reports in Genetics
|
May 30, 2019
Niemann-Pick Disease: An Underdiagnosed Lysosomal Storage Disorder
Inusha Panigrahi, Manoj Dhanorkar, Renu Suthar, et al.
Dermatologic Therapy
|
June 14, 2020
Managing syndromic congenital ichthyosis at a tertiary care institute-Genotype-phenotype correlations, and novel treatments
Garima Dabas, Rahul Mahajan, Dipankar De, et al.
Indian Journal of Pediatrics
|
January 30, 2022
Characterization of the CYP21A2 Gene Mutations in Children with Classic Congenital Adrenal Hyperplasia
Shaily Saraf, Priyanka Srivastava, Inusha Panigrahi, et al.
BMC Pregnancy and Childbirth
|
April 10, 2026
Quantitative proteomic profiling of placental extracellular vesicles in recurrent pregnancy loss reveals their role in feto-maternal crosstalk
Chitra Bhardwaj, Priyanka Srivastava, Ravi Pratap Singh Bhadoriya, et al.
Pediatric Endocrinology, Diabetes, and Metabolism
|
July 19, 2024
Clinical and molecular characterisation of children with monogenic obesity: a case series
Arun George, Santhosh Navi, Pamali Nanda, et al.
Heliyon
|
January 16, 2024
Neurofibromatosis type 1: Clinical characteristics and mutation spectrum in a North Indian cohort
Priyanka Srivastava, Shifali Gupta, Chitra Bamba, et al.
Frontiers in Genetics
|
June 1, 2023
Identification of genetic alterations in couples and their products of conceptions from recurrent pregnancy loss in North Indian population
Priyanka Srivastava, Chitra Bamba, Seema Chopra, et al.
Hematology (Amsterdam, Netherlands)
|
February 28, 2007
Cytochemical, immunophenotypic and ultrastructural characterization of acute leukemias: a prospective study of fifty cases: haematological malignancy
Tathagata Chatterjee, Inusha Panigrahi, Neerja Agrawal, et al.
European Journal of Haematology
|
February 6, 2010
Evaluation of the genetic basis of phenotypic heterogeneity in north Indian patients with thalassemia major
Nidhi Sharma, Reena Das, Jasbir Kaur, et al.
Clinical Dysmorphology
|
March 29, 2019
Phenotypic heterogeneity of kyphoscoliosis with vertebral and rib defects: a case series
Inusha Panigrahi, Suresh Kumar Angurana, Harish Varma, et al.
Page
of 16