Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ashish Chiddarwar"'
Autor:
Rashmi Dongerdiye, Meghana Bokde, Tejashree Anil More, Arati Saptarshi, Rati Devendra, Ashish Chiddarwar, Prashant Warang, Prabhakar Kedar
Publikováno v:
Annals of Hematology. 102:1029-1036
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e311bb23e128a8ba9595fc8c61a3d17c
https://doi.org/10.1007/s00277-023-05152-2
https://doi.org/10.1007/s00277-023-05152-2
Autor:
Prashant Warang, Prabhakar Kedar, Anuja Kulkarni, Rati Devendra, Ashish Chiddarwar, Vinod Gupta
Publikováno v:
Human Mutation. 41:737-748
NADH-cytochrome b5 reductase 3 deficiency is an important genetic cause of recessive congenital methemoglobinemia (RCM) and occurs worldwide in autosomal recessive inheritance. In this Mutation Update, we provide a comprehensive review of all the pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a6aad4cea3befea7a8affe5a59bc4a3
https://doi.org/10.1002/humu.23973
https://doi.org/10.1002/humu.23973
Autor:
Ashish Chiddarwar, Prashant Warang, Rashmi Dongerdiye, Vinod Gupta, Manisha Madkaikar, Prabhakar Kedar
Publikováno v:
Journal of Clinical Pathology. 72:81-85
Glucose-6-phosphate isomerase (GPI) deficiency is an autosomal recessive genetic disorder causing congenital haemolytic anaemia (CHA). Diagnosis of GPI deficiency by the biochemical method is unpredicted. Molecular diagnosis by identifying genetic mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a471725646e9cd5b530d0815777e77f0
https://doi.org/10.1136/jclinpath-2018-205420
https://doi.org/10.1136/jclinpath-2018-205420
Publikováno v:
Annals of Human Genetics. 81:11-19
Summary Objective: The present study was undertaken to investigate the genotype and allele frequencies of the variants in the four bilirubin metabolism genes (UGT1A1, OATP2, HMOX1, and BLVRA) and their association with hyperbilirubinemia. Material an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba3dfa46dbcd8f242f44863f3283175d
https://doi.org/10.1111/ahg.12179
https://doi.org/10.1111/ahg.12179
Autor:
Ashish Chiddarwar, Aniket Mohite, Vinod Gupta, Anshul Jadli, Rati Devendra, Prashant Warang, Darshana Mirgal, Prabhakar Kedar, Malay B. Mukherjee
Publikováno v:
Blood Cells, Molecules, and Diseases. 66:8-10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d92c1d2116efe39b82f5563cdd925eb3
https://doi.org/10.1016/j.bcmd.2017.07.002
https://doi.org/10.1016/j.bcmd.2017.07.002
Autor:
Ashish Chiddarwar, M. P. Singh, Purushottam Patel, Prabhakar Kedar, Pramod Mayekar, Rati Devendra, Harsha V. Hegde, Neelima Mishra, Naseem Ahmed, Vinodkumar Gupta, Malay B. Mukherjee, Rajasubramaniam Shanmugam, Prashant Warang, Neena Valecha, S.L. Hoti
Publikováno v:
Infection, Genetics and Evolution. 86:104597
Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common human erythroenzymopathy affecting around 10% of the world population. India is endemic for malaria and antimalarial drugs are known to induce haemolysis in G6PD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1be104b72089dc25822e4016fd7d48ee
https://doi.org/10.1016/j.meegid.2020.104597
https://doi.org/10.1016/j.meegid.2020.104597
Autor:
Vinod Gupta, Harsha Prasada, Rashmi Dongerdiye, Rati Devendra, Pooja Chilwirwar, Sunil Bhat, Manisha Madkaikar, S Chandrakala, Ashish Chiddarwar, Prashant Warang, Abhilasha Sampagar, Prabhakar Kedar
Publikováno v:
Indian journal of pediatrics. 86(8)
Glucose-6-phosphate isomerase (GPI) deficiency is an autosomal recessive genetic disorder causing hereditary non-spherocytic hemolytic anemia (HNSHA) coupled with a neurological disorder. The aim of this study was to identify GPI genetic defects in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23438f2d5128e57fdd8214d8db31bb1f
https://pubmed.ncbi.nlm.nih.gov/31183741
https://pubmed.ncbi.nlm.nih.gov/31183741
Publikováno v:
Molecular biology reports. 45(6)
The present study was undertaken to investigate genetic variations present in the coding regions of the UGT1A1 gene among the Gilbert’s syndrome patients. Analysis of genetic variations was performed by direct DNA sequencing among the patients that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61bb5e3cf0ef229b8106db9035f1f64c
https://pubmed.ncbi.nlm.nih.gov/30105552
https://pubmed.ncbi.nlm.nih.gov/30105552
Autor:
Rati Devendra, Kanjaksha Ghosh, Selma D'Silva, Prabhakar Kedar, Malay B. Mukherjee, Roshan B. Colah, Prashant Warang, Ashish Chiddarwar
Publikováno v:
Annals of hematology. 94(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56c59934574adecf632aa7031cc6bd23
https://pubmed.ncbi.nlm.nih.gov/24947795
https://pubmed.ncbi.nlm.nih.gov/24947795