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Gross Hematuria Caused by Intravesical Migration of a Forgotten Intrauterine Device: A Case Report and Literature Review

Research and reports in urology, 2022-08, Vol.14, p.291-296

2022

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GLI3‐related polydactyly: a review

Clinical genetics, 2017-11, Vol.92 (5), p.457-466

2017

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Climate of Online e-Learning During COVID-19 Pandemic in a Saudi Medical School: Students’ Perspective

Journal of medical education and curricular development, 2023-01, Vol.10, p.23821205231173492-23821205231173492

2023

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Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy

Clinical genetics, 2017-09, Vol.92 (3), p.327-331

2017

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A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes

Neurogenetics, 2024-07, Vol.25 (4), p.425-433

2024

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Congenital Microcephaly with a Simplified Gyral Pattern: Associated Findings and Their Significance

American journal of neuroradiology : AJNR, 2011-06, Vol.32 (6), p.1123-1129

2011

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Pellagra-like condition is xeroderma pigmentosum/Cockayne syndrome complex and niacin confers clinical benefit

Clinical genetics, 2015-01, Vol.87 (1), p.56-61

2015

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Rare variant in LAMA2 gene causing congenital muscular dystrophy in a Sudanese family. A case report

Acta myologica, 2019-03, Vol.38 (1), p.21-24

2019

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Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations

European journal of human genetics : EJHG, 2023-04, Vol.32 (10), p.1214-1226

2023

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Clinical characterization of the HOXA1 syndrome BSAS variant

Neurology, 2007-09, Vol.69 (12), p.1245-1253

2007

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Association of Adverse Childhood Experiences and Resilience With Obesity, High Blood Pressure, and Parental Report of Behavioral Health Symptoms in Children: A Cross Sectional Study

Global pediatric health, 2023-01, Vol.10, p.2333794X231159518-2333794X231159518

2023

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Measurement of the educational environment in MBBS teaching program, according to DREEM in College of Medicine, University of Bahri, Khartoum, Sudan

Advances in medical education and practice, 2018-01, Vol.9, p.617-622

2018

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Assessment of Treatment of Community Acquired Severe Pneumonia by Two Different Antibiotics

Journal of clinical and diagnostic research, 2016-05, Vol.10 (5), p.SC06-SC09

2016

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NPHP4 mutation is linked to cerebello-oculo-renal syndrome and male infertility

Clinical genetics, 2014-04, Vol.85 (4), p.371-375

2014

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The Salih Ataxia Mutation Impairs Rubicon Endosomal Localization

Cerebellum (London, England), 2013-12, Vol.12 (6), p.835-840

2013

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Expanding the clinical spectrum and allelic heterogeneity in van den Ende-Gupta syndrome

Clinical genetics, 2014-05, Vol.85 (5), p.492-494

2014

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Paraparésie spastique héréditaire à phénotype complexe avec mutation dans le gène FA2H : description de 5 cas

Revue neurologique, 2014-04, Vol.170, p.A152-A152

2014

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Unraveling the MRI‐Based Microstructural Signatures Behind Primary Progressive and Relapsing–Remitting Multiple Sclerosis Phenotypes

Journal of magnetic resonance imaging, 2022-01, Vol.55 (1), p.154-163

2022

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IFNG and IFNGR1 gene polymorphisms and susceptibility to post-kala-azar dermal leishmaniasis in Sudan

Genes and immunity, 2007-01, Vol.8 (1), p.75-78

2007

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Genetic investigation of 93 families with microphthalmia or posterior microphthalmos

Clinical genetics, 2018-06, Vol.93 (6), p.1210-1222

2018

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Congenital Myasthenic Syndrome Due to Homozygous CHRNE Mutations: Report of Patients in Arabia

Journal of neuro-ophthalmology, 2011-03, Vol.31 (1), p.42-47

2011

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Brain stem and cerebellar findings in Joubert syndrome

Journal of computer assisted tomography, 2006-01, Vol.30 (1), p.116-121

2006

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Optic disk and white matter abnormalities in a patient with a de novo 18p partial monosomy

Ophthalmic genetics, 2010-09, Vol.31 (3), p.147-154

2010

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Stroke in Saudi children. Epidemiology, clinical features and risk factors

Saudi medical journal, 2006-03, Vol.27 Suppl 1, p.S12

2006

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Ophthalmologlc abnormalities in a de novo terminal 6q deletion

Ophthalmic genetics, 2010-03, Vol.31 (1), p.1-11

2010

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Gross Hematuria Caused by Intravesical Migration of a Forgotten Intrauterine Device: A Case Report and Literature Review

GLI3‐related polydactyly: a review

Climate of Online e-Learning During COVID-19 Pandemic in a Saudi Medical School: Students’ Perspective

Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy

A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes

Congenital Microcephaly with a Simplified Gyral Pattern: Associated Findings and Their Significance

Pellagra-like condition is xeroderma pigmentosum/Cockayne syndrome complex and niacin confers clinical benefit

Rare variant in LAMA2 gene causing congenital muscular dystrophy in a Sudanese family. A case report

Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations

Clinical characterization of the HOXA1 syndrome BSAS variant

Association of Adverse Childhood Experiences and Resilience With Obesity, High Blood Pressure, and Parental Report of Behavioral Health Symptoms in Children: A Cross Sectional Study

Measurement of the educational environment in MBBS teaching program, according to DREEM in College of Medicine, University of Bahri, Khartoum, Sudan

Assessment of Treatment of Community Acquired Severe Pneumonia by Two Different Antibiotics

NPHP4 mutation is linked to cerebello-oculo-renal syndrome and male infertility

The Salih Ataxia Mutation Impairs Rubicon Endosomal Localization

Expanding the clinical spectrum and allelic heterogeneity in van den Ende-Gupta syndrome

Paraparésie spastique héréditaire à phénotype complexe avec mutation dans le gène FA2H : description de 5 cas

Unraveling the MRI‐Based Microstructural Signatures Behind Primary Progressive and Relapsing–Remitting Multiple Sclerosis Phenotypes

IFNG and IFNGR1 gene polymorphisms and susceptibility to post-kala-azar dermal leishmaniasis in Sudan

Genetic investigation of 93 families with microphthalmia or posterior microphthalmos

Congenital Myasthenic Syndrome Due to Homozygous CHRNE Mutations: Report of Patients in Arabia

Brain stem and cerebellar findings in Joubert syndrome

Optic disk and white matter abnormalities in a patient with a de novo 18p partial monosomy

Stroke in Saudi children. Epidemiology, clinical features and risk factors

Ophthalmologlc abnormalities in a de novo terminal 6q deletion

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