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Huma Arshad Cheema

Showing results (31-40 of 56) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|September 2, 2019
Mapping of IDUA gene variants in Pakistani patients with mucopolysaccharidosis type 1Muhammad Yasir Zahoor, Huma Arshad Cheema, Sadaqat Ijaz, et al.
Gene|September 12, 2012
Detection of common mutations in the GALT gene through ARMSUmair Mahmood, Muhammad Imran, Salma Iqbal Naik, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 23, 2020
Variability of clinical and biochemical phenotype in liver phosphorylase kinase deficiency with variants in the phosphorylase kinase (PHKG2) geneNadia Waheed, Anjum Saeed, Sadaqat Ijaz, et al.
Journal of Ayub Medical College, Abbottabad : JAMC|March 7, 2019
Vitamin D Intoxication In 7-Month-Old Infant With Recommended Daily Intake Of Vitamin DNadia Waheed, Huma Arshad Cheema, Anjum Saeed, et al.
Case Reports in Perinatal Medicine|May 5, 2025
Aromatase deficiency due to novel <i>CYP19A1</i> mutation: a rare cause of maternal and fetal virilizationAamir Naseem, Muhammad Zahid, Kashan Arshad, et al.
Hormone Research in Paediatrics|August 25, 2025
Clinical Spectrum of Primary Hypomagnesemia with Secondary Hypocalcemia due to TRPM6 MutationSommayya Aftab, Muhammad Nadeem Anjum, Nida Aslam, et al.
JPMA. the Journal of the Pakistan Medical Association|January 2, 2022
Very early onset inflammatory bowel disease: Spectrum of clinical presentation, diagnostic tools and outcome in childrenHuma Arshad Cheema, Nadia Waheed, Anjum Saeed, et al.
The Turkish Journal of Gastroenterology : the Official Journal of Turkish Society of Gastroenterology|August 21, 2023
Clinical and Genetic Description of Hereditary Chronic Pancreatitis in Pakistani ChildrenHuma Arshad Cheema, Zafar Fayyaz, Anjum Saeed, et al.
Journal of Ayub Medical College, Abbottabad : JAMC|July 17, 2017
Spontaneous Perforation Of Bile Duct, Clinical Presentation, Laboratory Work Up, Treatment And OutcomeHassan Suleman Malik, Huma Arshad Cheema, Zafar Fayyaz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 14, 2015
Direct sequencing of FAH gene in Pakistani tyrosinemia type 1 families reveals a novel mutationSadaqat Ijaz, Muhammad Yasir Zahoor, Muhammad Imran, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

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Pageof 6
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 2, 2019
Mapping of IDUA gene variants in Pakistani patients with mucopolysaccharidosis type 1Muhammad Yasir Zahoor, Huma Arshad Cheema, Sadaqat Ijaz, et al.
Gene|September 12, 2012
Detection of common mutations in the GALT gene through ARMSUmair Mahmood, Muhammad Imran, Salma Iqbal Naik, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 23, 2020
Variability of clinical and biochemical phenotype in liver phosphorylase kinase deficiency with variants in the phosphorylase kinase (PHKG2) geneNadia Waheed, Anjum Saeed, Sadaqat Ijaz, et al.
Journal of Ayub Medical College, Abbottabad : JAMC|March 7, 2019
Vitamin D Intoxication In 7-Month-Old Infant With Recommended Daily Intake Of Vitamin DNadia Waheed, Huma Arshad Cheema, Anjum Saeed, et al.
Case Reports in Perinatal Medicine|May 5, 2025
Aromatase deficiency due to novel <i>CYP19A1</i> mutation: a rare cause of maternal and fetal virilizationAamir Naseem, Muhammad Zahid, Kashan Arshad, et al.
Hormone Research in Paediatrics|August 25, 2025
Clinical Spectrum of Primary Hypomagnesemia with Secondary Hypocalcemia due to TRPM6 MutationSommayya Aftab, Muhammad Nadeem Anjum, Nida Aslam, et al.
JPMA. the Journal of the Pakistan Medical Association|January 2, 2022
Very early onset inflammatory bowel disease: Spectrum of clinical presentation, diagnostic tools and outcome in childrenHuma Arshad Cheema, Nadia Waheed, Anjum Saeed, et al.
The Turkish Journal of Gastroenterology : the Official Journal of Turkish Society of Gastroenterology|August 21, 2023
Clinical and Genetic Description of Hereditary Chronic Pancreatitis in Pakistani ChildrenHuma Arshad Cheema, Zafar Fayyaz, Anjum Saeed, et al.
Journal of Ayub Medical College, Abbottabad : JAMC|July 17, 2017
Spontaneous Perforation Of Bile Duct, Clinical Presentation, Laboratory Work Up, Treatment And OutcomeHassan Suleman Malik, Huma Arshad Cheema, Zafar Fayyaz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 14, 2015
Direct sequencing of FAH gene in Pakistani tyrosinemia type 1 families reveals a novel mutationSadaqat Ijaz, Muhammad Yasir Zahoor, Muhammad Imran, et al.
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