| Thirteen year retrospective review of the spectrum of inborn errors of metabolism presenting in a tertiary center in Saudi Arabia M Alfadhel, M Benmeakel, MA Hossain, F Al Mutairi, A Al Othaim, ... Orphanet journal of rare diseases 11, 1-12, 2016 | 89 | 2016 |
| Trade liberalisation and technical efficiency: evidence from Bangladesh manufacturing industries MA Hossain, ND Karunaratne Journal of Development Studies 40 (3), 87-114, 2004 | 84 | 2004 |
| Late-onset Krabbe disease is predominant in Japan and its mutant precursor protein undergoes more effective processing than the infantile-onset form MA Hossain, T Otomo, S Saito, K Ohno, H Sakuraba, Y Hamada, K Ozono, ... Gene 534 (2), 144-154, 2014 | 55 | 2014 |
| Exports and economic growth in Bangladesh: Has manufacturing exports become a new engine of export-led growth? M Hossain, N Dias Karunaratne The international trade journal 18 (4), 303-334, 2004 | 51 | 2004 |
| Autoimmune diabetes associated with pembrolizumab: a review of published case reports A Cheema, B Makadia, T Karwadia, R Bajwa, M Hossain World journal of oncology 9 (1), 1, 2018 | 44 | 2018 |
| Chaperone therapy for Krabbe disease: potential for late-onset GALC mutations MA Hossain, K Higaki, S Saito, K Ohno, H Sakuraba, E Nanba, Y Suzuki, ... Journal of human genetics 60 (9), 539-545, 2015 | 37 | 2015 |
| Isolated pyramidal tract impairment in the central nervous system of adult-onset Krabbe disease with novel mutations in the GALC gene S Tokushige, T Sonoo, R Maekawa, Y Shirota, R Hanajima, Y Terao, ... Brain and Development 35 (6), 579-581, 2013 | 19 | 2013 |
| Chemical chaperone treatment for galactosialidosis: Effect of NOEV on β-galactosidase activities in fibroblasts MA Hossain, K Higaki, M Shinpo, E Nanba, Y Suzuki, K Ozono, N Sakai Brain and Development 38 (2), 175-180, 2016 | 18 | 2016 |
| Genistein reduces heparan sulfate accumulation in human mucolipidosis II skin fibroblasts T Otomo, MA Hossain, K Ozono, N Sakai Molecular Genetics and Metabolism 105 (2), 266-269, 2012 | 18 | 2012 |
| Availability of fish species in fish markets and fish marketing in Noakhali district M Leela, MFU Zaman, AA Asif, MA Hossain Bangladesh. Journal of Entomology and Zoology Studies 6 (4), 1332-1344, 2018 | 17 | 2018 |
| Seroprevalence of brucellosis in small ruminants in selected area of Bangladash MJ Uddin, MS Rahman, SH Akter, MA Hossain, MT Islam, MA Islam, ... Korean Journal of Veterinary Service 30 (4), 511-525, 2007 | 17 | 2007 |
| Dysregulated DNA methylation of GLA gene was associated with dysfunction of autophagy H Yanagisawa, MA Hossain, T Miyajima, K Nagao, T Miyashita, Y Eto Molecular Genetics and Metabolism 126 (4), 460-465, 2019 | 15 | 2019 |
| Unfolded protein response is activated in Krabbe disease in a manner dependent on the mutation type K Irahara-Miyana, T Otomo, H Kondo, MA Hossain, K Ozono, N Sakai Journal of Human Genetics 63 (6), 699-706, 2018 | 15 | 2018 |
| Application of a diagnostic methodology by quantification of 26: 0 lysophosphatidylcholine in dried blood spots for Japanese newborn screening of X-linked adrenoleukodystrophy C Wu, T Iwamoto, J Igarashi, T Miyajima, MA Hossain, H Yanagisawa, ... Molecular Genetics and Metabolism Reports 12, 115-118, 2017 | 15 | 2017 |
| A combination of 7-ketocholesterol, lysosphingomyelin and bile acid-408 to diagnose Niemann-Pick disease type C using LC-MS/MS C Wu, T Iwamoto, MA Hossain, K Akiyama, J Igarashi, T Miyajima, Y Eto PloS one 15 (9), e0238624, 2020 | 14 | 2020 |
| Hemolytic anemia an unusual presentation of vitamin B12 deficiency A Cheema, J Bramson, R Bajwa, MA Hossain, A Asif J Hematol Thrombo Dis 6 (1), 1000285, 2018 | 13 | 2018 |
| A novel homozygous GALC mutation: very early onset and rapidly progressive Krabbe disease F Kardas, AS Uzak, MA Hossain, N Sakai, M Canpolat, A Yıkılmaz Gene 517 (1), 125-127, 2013 | 13 | 2013 |
| Future clinical and biochemical predictions of Fabry disease in females by methylation studies of the GLA gene MA Hossain, C Wu, H Yanagisawa, T Miyajima, K Akiyama, Y Eto Molecular Genetics and Metabolism Reports 20, 100497, 2019 | 12 | 2019 |
| The severe clinical phenotype for a heterozygous Fabry female patient correlates to the methylation of non-mutated allele associated with chromosome 10q26 deletion syndrome MA Hossain, H Yanagisawa, T Miyajima, C Wu, A Takamura, K Akiyama, ... Molecular Genetics and Metabolism 120 (3), 173-179, 2017 | 12 | 2017 |
| A case of adult-onset Pompe disease with cerebral stroke and left ventricular hypertrophy MA Hossain, T Miyajima, K Akiyama, Y Eto Journal of Stroke and Cerebrovascular Diseases 27 (11), 3046-3052, 2018 | 11 | 2018 |
Majid AlfadhelHead Genetics division, Department of Pediatrics, King Saud bin Abdulaziz University for HealthVerified email at ngha.med.sa