Search Results - "Tamanna, Nasrin"

Biochemical and histopathological profiling of Wistar rat treated with Brassica napus as a supplementary feed by Hasan, Kazi Md. Mahmudul, Tamanna, Nasrin, Haque, Md. Anwarul

“…Metabolic changes together with cardiovascular and hepatic factors are related to the development of diseases like myocardial lipidosis, heart disease, and…”
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Biallelic mutations in pakistani families with autosomal recessive prelingual nonsyndromic hearing loss by Choi, Hee Ji, Kanwal, Sumaira, Hameed, Rashid, Tamanna, Nasrin, Perveen, Shazia, Mahreen, Hina, Son, Wonseok, Lee, Kyung Suk, Chung, Ki Wha

“…Background Nonsyndromic autosomal recessive hearing loss (DFNB) is an etiologically heterogeneous disorder group showing a wide spectrum of onset ages and…”
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Hurst exponent approach through rescaled range analysis to study the time series of summer monsoon rainfall over northeast India by Pal, Srishti, Dutta, Shrutinil, Nasrin, Tamanna, Chattopadhyay, Surajit

“…The present work reports a study on the behavior of the time series of rainfall during the summer monsoon (June–September) in northeast India. It has been…”
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Recessive IGNE/I Mutations in Korean Nonaka Distal Myopathy Patients with or without Peripheral Neuropathy by Tamanna, Nasrin, Pi, Byung Kwon, Lee, Ah Jin, Kanwal, Sumaira, Choi, Byung-Ok, Chung, Ki Wha

“…Autosomal recessive Nonaka distal myopathy is a rare autosomal recessive genetic disease characterized by progressive degeneration of the distal muscles,…”
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Recessive GNE Mutations in Korean Nonaka Distal Myopathy Patients with or without Peripheral Neuropathy by Tamanna, Nasrin, Pi, Byung Kwon, Lee, Ah Jin, Kanwal, Sumaira, Choi, Byung-Ok, Chung, Ki Wha

“…Autosomal recessive Nonaka distal myopathy is a rare autosomal recessive genetic disease characterized by progressive degeneration of the distal muscles,…”
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Peripheral Myelin Protein 22 Gene Mutations in Charcot-Marie-Tooth Disease Type 1E Patients by Jung, Na Young, Kwon, Hye Mi, Nam, Da Eun, Tamanna, Nasrin, Lee, Ah Jin, Kim, Sang Beom, Choi, Byung-Ok, Chung, Ki Wha

“…Duplication and deletion of the peripheral myelin protein 22 (PMP22) gene cause Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy with…”
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Complete genome sequences of bacteria isolated from cockroaches collected in a Bangladeshi hospital by Workman, Sean D., Islam, Saiful, Akter, Shamima, Nasrin, Tamanna, Haque, Fazlul, Yost, Christopher K., Mohanta, Moni Krishno

“…ABSTRACT We report the complete genome sequences of four bacterial strains that were isolated from Blattella germanica (German cockroaches) that were found in…”
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