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Splenectomy vs. rituximab as a second-line therapy in immune thrombocytopenic purpura: a single center experience

International journal of hematology, 2018-01, Vol.107 (1), p.69-74

2018

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Clinical features and histopathological analysis of corneal myxoma

Scientific reports, 2022-07, Vol.12 (1), p.11207-11207, Article 11207

2022

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Vision related quality of life of patients with keratoconus after keratoplasty at a Tertiary Eye Hospital in Saudi Arabia

European journal of ophthalmology, 2021-11, Vol.31 (6), p.3500-3504

2021

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Familial Retinal Arterial Macroaneurysms with Peripheral Retinal Ischemia: A Characterization on Ultra-Widefield Fluorescein Angiography

Middle East African journal of ophthalmology, 2020-10, Vol.27 (4), p.228-230

2020

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Future ophthalmology practice pattern: A survey of Saudi Board of Ophthalmology residents

Saudi journal of ophthalmology, 2019-01, Vol.33 (1), p.1-6

2019

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APSC2015-1289 Cardiovascular Complications Among Amphetamine Users Admitted to King Abdul-Aziz Medical City in Riyadh Between January 2006 and December 2013

Global heart, 2015-06, Vol.10 (2), p.e5-e6

2015

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The effect of retentive interlocking on the push-out failure of fiber post/composite core system

The Saudi dental journal, 2019, Vol.31, p.S65-S66

2019

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Outcomes of Corneal Topography among Progressive Keratoconus Patients 12 months following Corneal Collagen Cross-Linking

Clinical ophthalmology (Auckland, N.Z.), 2021-01, Vol.15, p.49-55

2021

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A Novel Variant in CWF19L1 Gene in a Family with Late-Onset Autosomal Recessive Cerebellar Ataxia 17

Neurological research (New York), 2021-02, Vol.43 (2), p.141-147

2021

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A novel mutation in ATM gene in a Saudi female with ataxia telangiectasia

International journal of neuroscience, 2021-02, Vol.131 (2), p.206-211

2021

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Clinical profile, risk factors and outcomes of ric COVID-19: a retrospective cohort multicentre study in Saudi Arabia

BMJ open, 2022-03, Vol.12 (3), p.e053722-e053722

2022

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A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 gene

Seizure (London, England), 2019-07, Vol.69, p.133-139

2019

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Autosomal recessive cerebellar ataxia with spasticity due to a rare mutation in GBA2 gene in a large consanguineous Saudi family

Genes & diseases, 2021-01, Vol.8 (1), p.110-114

2021

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Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects

Pediatric cardiology, 2018-06, Vol.39 (5), p.924-940

2018

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A Bidirectional Arabic Sign Language Framework Using Deep Learning and Fuzzy Matching Score

Mathematics (Basel), 2024-04, Vol.12 (8), p.1155

2024

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A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

Journal of stroke and cerebrovascular diseases, 2020-07, Vol.29 (7), p.104832-104832, Article 104832

2020

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Pattern of Malignant Tumors in Najran, Saudi Arabia: A 5-year Retrospective Study

International journal of biomedicine, 2021-12, Vol.11 (4), p.498-504

2021

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INVESTIGATION OF IN VITRO GENOTOXIC EFFECTS OF MONOCROTOPHOS ON HUMAN SKIN KERATINOCYTE CELLS

Fresenius environmental bulletin, 2018-05, Vol.27 (5), p.2883

2018

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Epidemiology of non-transported emergency medical services calls in Saudi Arabia

Saudi medical journal, 2016-05, Vol.37 (5), p.575-578

2016

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A novel variant c.3706C>T p.(Avg 1236Cys) in the ABCA7 gene in a Saudi patient with susceptibility to Alzheimer's disease 9

Intractable & Rare Diseases Research, 2020/08/31, Vol.9(3), pp.151-155

2020

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A novel mutation in CACNA1A gene in a Saudi female with episodic ataxia type 2 with no response to acetazolamide or 4-aminopyridine

Intractable & Rare Diseases Research, 2019/02/28, Vol.8(1), pp.67-71

2019

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Ataxia with ocular apraxia type 2 not responding to 4-aminopyridine: A rare mutation in the SETX gene in a Saudi patient

Intractable & Rare Diseases Research, 2018/11/30, Vol.7(4), pp.275-279

2018

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A novel mutation in TTN gene in a Saudi patient with bilateral facial weakness and scapular winging

Intractable & Rare Diseases Research, 2019/05/31, Vol.8(2), pp.142-145

2019

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Congenital insensitivity to pain with anhidrosis: A report of two siblings with a novel mutation in (TrkA) NTRK1 gene in a Saudi family

Journal of the neurological sciences, 2016-11, Vol.370, p.35-38

2016

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Expanding the Donor Pool to the Ultimate Level: Introducing the Revolutionary Hybrid Dual Graft Liver Transplant Using Domino and Living Donors

Transplantation direct, 2024-08, Vol.10 (8), p.e1681

2024

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Splenectomy vs. rituximab as a second-line therapy in immune thrombocytopenic purpura: a single center experience

Clinical features and histopathological analysis of corneal myxoma

Vision related quality of life of patients with keratoconus after keratoplasty at a Tertiary Eye Hospital in Saudi Arabia

Familial Retinal Arterial Macroaneurysms with Peripheral Retinal Ischemia: A Characterization on Ultra-Widefield Fluorescein Angiography

Future ophthalmology practice pattern: A survey of Saudi Board of Ophthalmology residents

APSC2015-1289 Cardiovascular Complications Among Amphetamine Users Admitted to King Abdul-Aziz Medical City in Riyadh Between January 2006 and December 2013

The effect of retentive interlocking on the push-out failure of fiber post/composite core system

Outcomes of Corneal Topography among Progressive Keratoconus Patients 12 months following Corneal Collagen Cross-Linking

A Novel Variant in CWF19L1 Gene in a Family with Late-Onset Autosomal Recessive Cerebellar Ataxia 17

A novel mutation in ATM gene in a Saudi female with ataxia telangiectasia

Clinical profile, risk factors and outcomes of ric COVID-19: a retrospective cohort multicentre study in Saudi Arabia

A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 gene

Autosomal recessive cerebellar ataxia with spasticity due to a rare mutation in GBA2 gene in a large consanguineous Saudi family

Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects

A Bidirectional Arabic Sign Language Framework Using Deep Learning and Fuzzy Matching Score

A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

Pattern of Malignant Tumors in Najran, Saudi Arabia: A 5-year Retrospective Study

INVESTIGATION OF IN VITRO GENOTOXIC EFFECTS OF MONOCROTOPHOS ON HUMAN SKIN KERATINOCYTE CELLS

Epidemiology of non-transported emergency medical services calls in Saudi Arabia

A novel variant c.3706C>T p.(Avg 1236Cys) in the ABCA7 gene in a Saudi patient with susceptibility to Alzheimer's disease 9

A novel mutation in CACNA1A gene in a Saudi female with episodic ataxia type 2 with no response to acetazolamide or 4-aminopyridine

Ataxia with ocular apraxia type 2 not responding to 4-aminopyridine: A rare mutation in the SETX gene in a Saudi patient

A novel mutation in TTN gene in a Saudi patient with bilateral facial weakness and scapular winging

Congenital insensitivity to pain with anhidrosis: A report of two siblings with a novel mutation in (TrkA) NTRK1 gene in a Saudi family

Expanding the Donor Pool to the Ultimate Level: Introducing the Revolutionary Hybrid Dual Graft Liver Transplant Using Domino and Living Donors

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