Zobrazeno 1 - 10
of 22
pro vyhledávání: '"C. Muhizi"'
Autor:
N. Dukuze, E. Uwibambe, P. Sesonga, J. Niyongere, B. Tuyishimire, A. Urungwiro, J. Ndinkabandi, A. Rwamatwara, S. Niyoyita, G. Isingizwe, J. Mutamuliza, C. Nsanzabaganwa, J. Bukuru, F. Rutagarama, O. Karangwa, A. Ndatinya, C. Muhizi, L. Mutesa
Publikováno v:
Rwanda Medical Journal, Vol 80, Iss 4 (2024)
Usher syndrome is a genetic, clinically heterogeneous condition characterized by sensorineural hearing loss, progressive retinal degeneration, and vestibular dysfunction. There are three phenotypically recognizable types of Usher syndrome. Individual
Externí odkaz:
https://doaj.org/article/aa3217732de745fdad0923d22316ac00
Autor:
B. Tuyishimire, H. Irere, N. Dukuze, B. Iradukunda, C. Muhizi, O. R. Karangwa, F. Rutagarama, C. Nsanzabaganwa, L. Mutesa
Publikováno v:
Rwanda Medical Journal, Vol 80, Iss 1, Pp 5-8 (2023)
INTRODUCTION: While Beckwith-Wiedemann syndrome is among rare genomic imprinting disorders, its diagnosis still presents challenges in clinical settings. Therefore, the aim of this work is to present different phenotypic features of this syndrome. CA
Externí odkaz:
https://doaj.org/article/36dcda8ce2114623a50b6ae23a608367
Autor:
C. Muhizi, H. Irere, B. Tuyishimire, A. Ndatinya, O. R. Karangwa, F. Rutagarama, C. Nsanzabaganwa, L. Mutesa
Publikováno v:
Rwanda Medical Journal, Vol 79, Iss 4, Pp 5-8 (2022)
INTRODUCTION: Neurofibromatosis Type 1 (NF1) or Von Recklinghausen’s disease, is a rare genetic disease characterized by multiple benign tumors of nerves and skin (neurofibromas), and skin decorations. However, it is multisystem and can affect each
Externí odkaz:
https://doaj.org/article/8bc1a5d5c5714643bd41121dc910d626
Autor:
B. Tuyishimire, H. Irere, C. Muhizi, A. Ndatinya, O. R. Karangwa, F. Rutagarama, C. Nsanzabaganwa, L. Mutesa
Publikováno v:
Rwanda Medical Journal, Vol 79, Iss 4, Pp 9-12 (2022)
INTRODUCTION: Although Treacher-Collins syndrome has to be considered a differential diagnosis in congenital craniofacial abnormalities, the clinical diagnosis and research related to it still present a gap, especially in African regions. Thus, this
Externí odkaz:
https://doaj.org/article/a8b0d83bb7e44a649e62e7c29016d74c
Autor:
B. Tuyishimire, H. Irere, C. Muhizi, A. Ndatinya, O. R. Karangwa, F. Rutarama, C. Nsanzabaganwa, L. Mutesa
Publikováno v:
Rwanda Medical Journal, Vol 79, Iss 4 (2022)
INTRODUCTION: Although Treacher-Collins syndrome has to be considered a differential diagnosis in congenital craniofacial abnormalities, the clinical diagnosis and research related to it still present a gap, especially in African regions. Thus, this
Externí odkaz:
https://doaj.org/article/52e989ce09e7439d9e5934780ffd599a
Publikováno v:
International Journal of Advanced Research. 9:402-410
Objective: To determine the prevalence and risk factors associated with type 2 diabetic retinopathy in Rwanda. Methods: A case-control study was conducted from January to September 2019 in four hospitals within the Republic of Rwanda. Type 2 diabetic
Objective:To determine the prevalence and risk factors associated with type 2 diabetic retinopathy in Rwanda. Methods:A case-control study was conducted from January to September 2019 in four hospitals within the Republic of Rwanda. Type 2 diabetic p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4f19f031f0a390e2eb2818fca585f01
— Background: Diabetic nephropathy is an emerging clinical and public problem and is related with poor outcomes such as heart failure, and end stage renal disease. In the Rwanda countryside there are no recent studies on renal complications. Object
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2772ff36255d2f4e4803bfe0a8d6e9b0
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Akademický článek
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