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Huma Arshad Cheema

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Clinical Biochemistry|May 31, 2019
Spectrum of UGT1A1 variants in Pakistani children affected with inherited unconjugated hyperbilirubinemiasBibi Zubaida, Huma Arshad Cheema, Muhammad Almas Hashmi, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|June 30, 2016
Spectrum of Inherited Metabolic Disorders in Pakistani Children Presenting at a Tertiary Care CentreHuma Arshad Cheema, Hassan Suleman Malik, Arit Parkash, et al.
Human Heredity|October 19, 2020
Novel IDS Variants Identified in Three Unrelated Pakistani Patients Affected with Mucopolysaccharidosis Type II (Hunter Syndrome)Bibi Zubaida, Hajira Batool, Huma Arshad Cheema, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|September 28, 2016
Chanarin-Dorfman SyndromeNadia Waheed, Huma Arshad Cheema, Hassan Suleman, et al.
JPMA. the Journal of the Pakistan Medical Association|May 14, 2020
Haemobilia: secondary to micro aneurysms of hepatic arteryIqra Mushtaq, Huma Arshad Cheema, Hassan Suleman Malik, et al.
Journal of Ayub Medical College, Abbottabad : JAMC|July 17, 2017
Clinical Spectrum Of Solitary Rectal Ulcer In Children Presenting With Per-Rectal BleedMuhammad Nadeem Anjum, Huma Arshad Cheema, Hassan Suleman Malik, et al.
Pakistan Journal of Medical Sciences|April 16, 2020
Mutational spectrum of <i>SMPD1</i> gene in Pakistani Niemann-Pick disease patientsHuma Arshad Cheema, Iqra Ghulam Rasool, Muhammad Nadeem Anjum, et al.
Cureus|June 19, 2023
Corticosterone Methyl Oxidase Type 1 (CMO1) Deficiency Due to CYP11B2 Mutation: Two Case ReportsSaad Ur Rehman, Sommayya Aftab, Aamir Naseem, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 3, 2020
Identification of two novel variants in GNPTAB underlying mucolipidosis II in a Pakistani familyMuhammad Aman Khan, Bibi Zubaida, Noreen Karim, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|April 26, 2018
Is Hepatovenocaval Syndrome a Different Entity from Budd-Chiari Syndrome in Children?Nadia Waheed, Huma Arshad Cheema, Hassan Suleman, et al.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
Clinical Biochemistry|May 31, 2019
Spectrum of UGT1A1 variants in Pakistani children affected with inherited unconjugated hyperbilirubinemiasBibi Zubaida, Huma Arshad Cheema, Muhammad Almas Hashmi, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|June 30, 2016
Spectrum of Inherited Metabolic Disorders in Pakistani Children Presenting at a Tertiary Care CentreHuma Arshad Cheema, Hassan Suleman Malik, Arit Parkash, et al.
Human Heredity|October 19, 2020
Novel IDS Variants Identified in Three Unrelated Pakistani Patients Affected with Mucopolysaccharidosis Type II (Hunter Syndrome)Bibi Zubaida, Hajira Batool, Huma Arshad Cheema, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|September 28, 2016
Chanarin-Dorfman SyndromeNadia Waheed, Huma Arshad Cheema, Hassan Suleman, et al.
JPMA. the Journal of the Pakistan Medical Association|May 14, 2020
Haemobilia: secondary to micro aneurysms of hepatic arteryIqra Mushtaq, Huma Arshad Cheema, Hassan Suleman Malik, et al.
Journal of Ayub Medical College, Abbottabad : JAMC|July 17, 2017
Clinical Spectrum Of Solitary Rectal Ulcer In Children Presenting With Per-Rectal BleedMuhammad Nadeem Anjum, Huma Arshad Cheema, Hassan Suleman Malik, et al.
Pakistan Journal of Medical Sciences|April 16, 2020
Mutational spectrum of <i>SMPD1</i> gene in Pakistani Niemann-Pick disease patientsHuma Arshad Cheema, Iqra Ghulam Rasool, Muhammad Nadeem Anjum, et al.
Cureus|June 19, 2023
Corticosterone Methyl Oxidase Type 1 (CMO1) Deficiency Due to CYP11B2 Mutation: Two Case ReportsSaad Ur Rehman, Sommayya Aftab, Aamir Naseem, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 3, 2020
Identification of two novel variants in GNPTAB underlying mucolipidosis II in a Pakistani familyMuhammad Aman Khan, Bibi Zubaida, Noreen Karim, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|April 26, 2018
Is Hepatovenocaval Syndrome a Different Entity from Budd-Chiari Syndrome in Children?Nadia Waheed, Huma Arshad Cheema, Hassan Suleman, et al.
Pageof 6