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Anas M Alazami

Showing results (11-20 of 66) with videos related to

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Molecular Genetics & Genomic Medicine|April 2, 2014
Novel IFT122 mutation associated with impaired ciliogenesis and cranioectodermal dysplasiaAnas M Alazami, Mohammed Zain Seidahmed, Fatema Alzahrani, et al.
American Journal of Medical Genetics. Part A|December 15, 2012
Weaver syndrome and defective cortical development: a rare associationAhmed Al-Salem, Muneera J Alshammari, Hamdy Hassan, et al.
Human Genetics|November 29, 2018
A novel ISLR2-linked autosomal recessive syndrome of congenital hydrocephalus, arthrogryposis and abdominal distensionAnas M Alazami, Sateesh Maddirevula, Mohamed Zain Seidahmed, et al.
Journal of Clinical Immunology|January 27, 2025
Hematopoietic Stem Cell Transplantation Corrects IL-2Rβ DeficiencyFai AlQahtani, Manar AlGhamdi, Mofareh AlZahrani, et al.
Heliyon|February 2, 2024
<i>Calotropis procera:</i> A double edged sword against glioblastoma, inhibiting glioblastoma cell line growth by targeting histone deacetylases (HDAC) and angiogenesisShamsa Hilal Saleh Alanazi, Muhammad Farooq Khan, Anas M Alazami, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Congenital disorder of glycosylation IIa: the trouble with diagnosing a dysmorphic inborn error of metabolismAnas M Alazami, Dorota Monies, Brian F Meyer, et al.
Clinical and Experimental Rheumatology|January 31, 2017
Evolving spectrum of LRBA deficiency-associated chronic arthritis: is there a causative role in juvenile idiopathic arthritis?Sulaiman M Al-Mayouf, Hamzah Naji, Khalid Alismail, et al.
Journal of Medical Genetics|March 10, 2015
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18BAnas M Alazami, Amal Y Kentab, Eissa Faqeih, et al.
International Journal of Rheumatic Diseases|November 9, 2017
Monogenic interferonopathies: Phenotypic and genotypic findings of CANDLE syndrome and its overlap with C1q deficient SLESulaiman M Al-Mayouf, Alhanouf AlSaleem, Nora AlMutairi, et al.
Journal of Clinical Immunology|August 25, 2019
STK4 Deficiency in a Patient with Immune Complex Glomerulonephritis, Salt-Losing Tubulopathy, and Castleman's-Like DiseaseBandar Al-Saud, Huda Alajlan, Haneen Sabar, et al.
Pageof 7

Showing results (11-20 of 66) with videos related to

Sort By:
Pageof 7
Molecular Genetics & Genomic Medicine|April 2, 2014
Novel IFT122 mutation associated with impaired ciliogenesis and cranioectodermal dysplasiaAnas M Alazami, Mohammed Zain Seidahmed, Fatema Alzahrani, et al.
American Journal of Medical Genetics. Part A|December 15, 2012
Weaver syndrome and defective cortical development: a rare associationAhmed Al-Salem, Muneera J Alshammari, Hamdy Hassan, et al.
Human Genetics|November 29, 2018
A novel ISLR2-linked autosomal recessive syndrome of congenital hydrocephalus, arthrogryposis and abdominal distensionAnas M Alazami, Sateesh Maddirevula, Mohamed Zain Seidahmed, et al.
Journal of Clinical Immunology|January 27, 2025
Hematopoietic Stem Cell Transplantation Corrects IL-2Rβ DeficiencyFai AlQahtani, Manar AlGhamdi, Mofareh AlZahrani, et al.
Heliyon|February 2, 2024
<i>Calotropis procera:</i> A double edged sword against glioblastoma, inhibiting glioblastoma cell line growth by targeting histone deacetylases (HDAC) and angiogenesisShamsa Hilal Saleh Alanazi, Muhammad Farooq Khan, Anas M Alazami, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Congenital disorder of glycosylation IIa: the trouble with diagnosing a dysmorphic inborn error of metabolismAnas M Alazami, Dorota Monies, Brian F Meyer, et al.
Clinical and Experimental Rheumatology|January 31, 2017
Evolving spectrum of LRBA deficiency-associated chronic arthritis: is there a causative role in juvenile idiopathic arthritis?Sulaiman M Al-Mayouf, Hamzah Naji, Khalid Alismail, et al.
Journal of Medical Genetics|March 10, 2015
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18BAnas M Alazami, Amal Y Kentab, Eissa Faqeih, et al.
International Journal of Rheumatic Diseases|November 9, 2017
Monogenic interferonopathies: Phenotypic and genotypic findings of CANDLE syndrome and its overlap with C1q deficient SLESulaiman M Al-Mayouf, Alhanouf AlSaleem, Nora AlMutairi, et al.
Journal of Clinical Immunology|August 25, 2019
STK4 Deficiency in a Patient with Immune Complex Glomerulonephritis, Salt-Losing Tubulopathy, and Castleman's-Like DiseaseBandar Al-Saud, Huda Alajlan, Haneen Sabar, et al.
Pageof 7