Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Marukh Wadia"'
Autor:
Kanjaksha Ghosh, Marukh Wadia, Reema Surve, Pratibha Sawant, Khushnooma Italia, Anita Nadkarni, Roshan B. Colah
Publikováno v:
European Journal of Haematology. 89:160-164
Objectives To study the varied clinical and haematological profile of β-thalassaemia homozygotes, compound heterozygotes and heterozygotes with the Poly A (TC) mutation and its implication in prenatal diagnosis. Materials and methods Forty individua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70a59d842cd23ba2c67fabfaec7d559d
https://doi.org/10.1111/j.1600-0609.2012.01810.x
https://doi.org/10.1111/j.1600-0609.2012.01810.x
Autor:
Dipika Mohanty, Pramod Mayekar, Prakash Solanki, Reema Surve, Ajit Gorakshakar, Marukh Wadia, Adi Dastur, Roshan B. Colah, Mariamma Thomas
Publikováno v:
Genetic Testing. 12:181-185
Premarital screening for beta-thalassemia is not widely acceptable in India; hence, we evaluated the effectiveness of antenatal screening and counseling over 7 years.61,935 pregnant women were screened using the single-tube osmotic fragility test dur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb380082a5129b40be4d42e31e0190b2
https://doi.org/10.1089/gte.2007.0066
https://doi.org/10.1089/gte.2007.0066
Autor:
Marukh Wadia, Ajit Gorakshakar, Roshan B. Colah, Dipika Mohanty, Anita Nadkarni, Ryoiti Kiyama
Publikováno v:
Hemoglobin. 32:425-433
delta beta-Thalassemia (delta beta-thal) and hereditary persistence of fetal hemoglobin (HPFH) are heterogeneous disorders characterized by elevated levels of Hb F in adult life. The two disorders should not be considered as unambiguously separate en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32632302dc5399a9850730cfc9628192
https://doi.org/10.1080/03630260802341687
https://doi.org/10.1080/03630260802341687
Publikováno v:
International journal of laboratory hematology. 32(1 Pt 1)
Accurate estimation of hemoglobin (Hbs) A, Hb A(2), Hb F and abnormal Hb is required for diagnosis of hemoglobinopathies and genetic counseling. High pressure liquid chromatography (HPLC) is the most suitable approach available. But for 70% of the ru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51e600f8130306dcce5bafa4df9c1a3c
https://pubmed.ncbi.nlm.nih.gov/18727652
https://pubmed.ncbi.nlm.nih.gov/18727652
Autor:
K. M. Murhekar, Mohanty D, Marukh Wadia, Roshan B. Colah, A. C. Gorakshakar, M. V. Murhekar, Supriya Phanasgaonkar, Reema Surve, Malay B. Mukherjee, S Shridevi
Publikováno v:
Human biology. 73(5)
The Great Andamanese are a primitive Negrito tribe of the Andaman and Nicobar Islands, India, with a total population of 37. We studied 29 individuals from eight families from this population for abnormal hemoglobins, G6PD deficiency, DNA haplotypes,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9211f1900d1f9c069bba7b7adb483a53
https://pubmed.ncbi.nlm.nih.gov/11758693
https://pubmed.ncbi.nlm.nih.gov/11758693