Search Results - "Salih, M.A.M"

FP54-FR-05 Genotype and phenotype study in Sudanese and Yemeni families with axonal recessive Charcot-Marie-Tooth disease by Salih, M.A.M, Mikesova, E, Elmalik, S.A, Mukhtar, M.M, LeGuern, E, Azzedine, H

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PO19-WE-05 Linkage analysis and mutation screening in PANK2 and PLA2G6 genes in 7 consanguineous Saudi Arabian families with Karak syndrome by Azzedine, H, Salih, M.A.M, Khan, A, Mundwiller, E, Aldriss, A, Elmalik, S.A, Kabiraj, M.M, Stevanin, G

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P1.16 Novel mutations and loci are associated with limb girdle muscular dystrophy type 2 by Boyden, S.E, Salih, M.A.M, Estrella, E.A, White, A.J, Duncan, A.R, Burgess, S.L, Seidahmed, M.Z, Bennett, R.R, Kunkel, L.M, Kang, P.B

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EM.P.2.04 Unraveling the genetic complexity of alpha-dystroglycanopathies: Ethnically diverse pathogenic mutations by Manzini, M.C, Gleason, D, Chang, B.S, Hill, R.S, Partlow, J.N, Barry, B.J, Poduri, A, Basel-Vanagaite, L, Seidhamed, M.Z, Salih, M.A.M, Dobyns, W.B, Walsh, C.A

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REFINEMENT OF THE CLINICAL PHENOTYPE IN MUSK-RELATED CONGENITAL MYASTHENIC SYNDROMES by MIHAYLOVA, V, SALIH, M. A. M, LOCHMÜLLER, H, GUERGUELTCHEVA, V, MUKHTAR, M. M, ABUZEID, H. A, EL-SADIG, S. M, VON DER HAGEN, M, HUEBNER, A, NÜRNBERG, G, ABICHT, A, MÜLLER, J. S

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Genetic polymorphisms of fecundity genes in Watish Sudanese desert sheep by Mohamed, Sara E Ibrahim, Ahmed, Romaz M, Jawasreh, Khaleel I Z, Salih, M A M, Abdelhalim, Dalia Mursi, Abdelgadir, A W, Obeidat, Md T, Musa, L M A, Ahmed, Mohammed-Khair A

“…The Watish sheep is a strain of desert sheep of smaller size compared to other desert sheep ecotypes, and there is anecdotal evidence that it is endowed with…”
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Government policy and options in pastoral development in the Sudan by Salih, M.A.M. (Nordiska Afrikainst., Uppsala (Sweden))

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Pastoralism and the state in African arid lands. An overview by Salih, M.A.M. (Nordiska Afrikainst., Uppsala (Sweden))

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Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25 by JEN, J, COULIN, C. J, BOSLEY, T. M, SALIH, M. A. M, SABATTI, C, NELSON, S. F, BALOH, R. W

“…Horizontal gaze palsy with progressive scoliosis (HGPS) is a rare, autosomal recessive disorder characterized by a congenital absence of conjugate horizontal…”
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Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity by Salih, M A, Maisonobe, T, Kabiraj, M, al Rayess, M, al-Turaiki, M H, Akbar, M, Tahan, A, Urtizberea, J A, Grid, D, Hamadouche, T, Guilbot, A, Brice, A, Leguern, E

“…We describe a six generation Saudi kindred, with a recessive hereditary motor and sensory neuropathy (HMSN). Four individuals were affected including two…”
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Moyamoya syndrome with unusual angiographic findings and protein C deficiency: Review of the literature by Andeejani, A.M.I, Salih, M.A.M, Kolawole, T, Gader, AMA, Malabarey, T.O, Al Damegh, S, Al Boukai, A

“…We describe the findings in a six-year-old female with typical clinical symptoms of Moyamoya phenomena, but with an unusual angiographic appearance. The…”
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Etudes sur les caractéristiques de l'agent causal Mycobacterium farcinogenes du farcin du bouf au Soudan by El Sanousi, S.M., Salih, M.A.M., Mousa, M.T., Tag el Din, M.H., Soad, A.M.A.

“…Le farcin du boeuf a fait l'objet d'enquêtes dans trois départements du Soudan, de janvier à avril 1978, qui ont montré que l'affection atteignait 5,19 p. 100…”
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Genetic Refinement And Physical Mapping Of The CMT4B Gene On Chromosome 11Q22 by Bolino, A., Levy, E.R., Muglia, M., Conforti, F.L., LeGuern, E., Salih, M.A.M., Georgiou, D.M., Hausmanowa‐Petrusewicz, I., Mandich, P., Gambardella, A., Quattrone, A., Devoto, M., Monaco, A.P.

“…Charcot‐Marie‐Tooth disease type 4B (CMT4B) is a demyelinating autosomal recessive motor and sensory neuropathy characterized by focally folded myelin sheaths…”
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AIDS and HIV infection in Sudanese children: a clinical and epidemiological study by Hashim, M S, Salih, M A, el Hag, A A, Karrar, Z A, Osman, E M, el-Shiekh, F S, el Tilib, I A, Attala, N E

“…HIV surveillance and screening programs were established at Khartoum Teaching Hospital (KTH) following the first identified HIV case diagnosed in a hemophiliac…”
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An ELISA assay for the rapid diagnosis of acute bacterial meningitis by Salih, M A, Ahmed, A A, Sid Ahmed, H, Olcen, P

“…A recently introduced ELISA test (EIA-Test) was used for the detection of the common organisms that cause acute bacterial meningitis (ABM). The test--which…”
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Case of partial trisomy 2q3 with clinical manifestations of Marshall-Smith syndrome by Seidahmed, M. Zein, Rooney, D.E., Salih, M.A.M., Basit, O. Bashir Abdel, Shaheed, M.M., Abdullah, M.A., Abomelha, A.

“…We describe a girl with physical anomalies, accelerated skeletal maturation, failure to thrive, and respiratory difficulties consistent with a diagnosis of…”
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Miliary bovine farcy experimentally induced in a Zebu calf by El Sanousi, S M, Salih, M A

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Multiple congenital malformations in two sibs reminiscent of hydrolethalus and pseudotrisomy 13 syndromes by Dincsoy, M Y, Salih, M A, al-Jurayyan, N, al Saadi, M, Patel, P J

“…We report on two sibs, born to consanguineous parents, with defects of the midline including cleft lip and palate, flat nose, hypotelorism, and dysgenesis of…”
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Further studies on the properties of the aetiology of bovine farcy isolated from Sudanese cattle by El Sanousi, S.M, Salih, M.A.M, Mousa, M.T, Tag El Din, M.H, Ali, S.A.M

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