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FP54-FR-05 Genotype and phenotype study in Sudanese and Yemeni families with axonal recessive Charcot-Marie-Tooth disease

Journal of the neurological sciences, 2009, Vol.285, p.S144-S144

2009

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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

Journal of the neurological sciences, 2009, Vol.285, p.S266-S266

2009

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P1.16 Novel mutations and loci are associated with limb girdle muscular dystrophy type 2

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.604-605

2010

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EM.P.2.04 Unraveling the genetic complexity of alpha-dystroglycanopathies: Ethnically diverse pathogenic mutations

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.552-553

2009

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Refinement of the clinical phenotype in musk-related congenital myasthenic syndromes

Neurology, 2009-12, Vol.73 (22), p.1926-1928

2009

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Genetic polymorphisms of fecundity genes in Watish Sudanese desert sheep

Veterinary World, 2020-04, Vol.13 (4), p.614-621

2020

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Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25

Neurology, 2002-08, Vol.59 (3), p.432-435

2002

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Government policy and options in pastoral development in the Sudan

Nomadic peoples, 1990, Vol.25 (25-27), p.65-78

Salih, M.A.M. (Nordiska Afrikainst., Uppsala (Sweden))

1990

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Pastoralism and the state in African arid lands. An overview

Nomadic peoples, 1990, Vol.25 (25-27), p.7-18

Salih, M.A.M. (Nordiska Afrikainst., Uppsala (Sweden))

1990

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Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity

Neuromuscular disorders : NMD, 2000-01, Vol.10 (1), p.10-15

2000

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Moyamoya syndrome with unusual angiographic findings and protein C deficiency: Review of the literature

Journal of the neurological sciences, 1998-07, Vol.159 (1), p.11-16

1998

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Genetic Refinement And Physical Mapping Of The CMT4B Gene On Chromosome 11Q22

Journal of the peripheral nervous system, 2000-06, Vol.5 (2), p.116-116

2000

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Etudes sur les caractéristiques de l'agent causal Mycobacterium farcinogenes du farcin du bouf au Soudan

Revue d'élevage et de médecine vétérinaire des pays tropicaux, 1979-02, Vol.32 (2), p.135

1979

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AIDS and HIV infection in Sudanese children: a clinical and epidemiological study

AIDS patient care and STDs, 1997-10, Vol.11 (5), p.331-337

1997

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An ELISA assay for the rapid diagnosis of acute bacterial meningitis

Annals of tropical paediatrics, 1995-12, Vol.15 (4), p.273-278

1995

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Case of partial trisomy 2q3 with clinical manifestations of Marshall-Smith syndrome

American journal of medical genetics, 1999-07, Vol.85 (2), p.185-188

1999

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Miliary bovine farcy experimentally induced in a Zebu calf

Veterinary pathology, 1979-05, Vol.16 (3), p.372-373

1979

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Multiple congenital malformations in two sibs reminiscent of hydrolethalus and pseudotrisomy 13 syndromes

American journal of medical genetics, 1995-04, Vol.56 (3), p.317-321

1995

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Further studies on the properties of the aetiology of bovine farcy isolated from Sudanese cattle

Revue d'élevage et de médecine vétérinaire des pays tropicaux, 1979, Vol.32 (2), p.135-141

1979

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Rockall score of the acute upper gastrointestinal bleeding patients the experience in Sudan

Sudan journal of medical sciences, 2009-11, Vol.4 (3)

2009

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Louse-borne relapsing fever: I. A clinical and laboratory study of 363 cases in the Sudan

Transactions of the Royal Society of Tropical Medicine and Hygiene, 1977, Vol.71 (1), p.43-48

1977

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FP54-FR-05 Genotype and phenotype study in Sudanese and Yemeni families with axonal recessive Charcot-Marie-Tooth disease

PO19-WE-05 Linkage analysis and mutation screening in PANK2 and PLA2G6 genes in 7 consanguineous Saudi Arabian families with Karak syndrome

P1.16 Novel mutations and loci are associated with limb girdle muscular dystrophy type 2

EM.P.2.04 Unraveling the genetic complexity of alpha-dystroglycanopathies: Ethnically diverse pathogenic mutations

Refinement of the clinical phenotype in musk-related congenital myasthenic syndromes

Genetic polymorphisms of fecundity genes in Watish Sudanese desert sheep

Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25

Government policy and options in pastoral development in the Sudan

Pastoralism and the state in African arid lands. An overview

Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity

Moyamoya syndrome with unusual angiographic findings and protein C deficiency: Review of the literature

Genetic Refinement And Physical Mapping Of The CMT4B Gene On Chromosome 11Q22

Etudes sur les caractéristiques de l'agent causal Mycobacterium farcinogenes du farcin du bouf au Soudan

AIDS and HIV infection in Sudanese children: a clinical and epidemiological study

An ELISA assay for the rapid diagnosis of acute bacterial meningitis

Case of partial trisomy 2q3 with clinical manifestations of Marshall-Smith syndrome

Miliary bovine farcy experimentally induced in a Zebu calf

Multiple congenital malformations in two sibs reminiscent of hydrolethalus and pseudotrisomy 13 syndromes

Further studies on the properties of the aetiology of bovine farcy isolated from Sudanese cattle

Rockall score of the acute upper gastrointestinal bleeding patients the experience in Sudan

Louse-borne relapsing fever: I. A clinical and laboratory study of 363 cases in the Sudan

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