Zafar Fayyaz
Overview
Explore the profile of Zafar Fayyaz including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
64
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Recent Articles
1.
Cheema H, Waheed N, Saeed A, Anjum M, Fayyaz Z, Ijaz S
J Pak Med Assoc
. 2023 Sep;
73(8):1610-1621.
PMID: 37697751
Objectives: To report the mutational landscape of a clinically diagnosed cohort of paediatric patients with cholestasis liver diseases. Methods: The retrospective study was conducted at the University of Child Health...
2.
Cheema H, Fayyaz Z, Saeed A, Anjum M, Ijaz S, Alvi M, et al.
Turk J Gastroenterol
. 2023 Aug;
34(10):1088-1098.
PMID: 37603299
Background/aims: The purpose of this study was to identify the spectrum and frequency of pathogenic variants as well as the clinical and genetic insight of hereditary chronic pancreatitis in Pakistani...
3.
Cheema H, Waheed N, Saeed A, Fayyaz Z, Anjum M, Alvi M, et al.
J Pak Med Assoc
. 2022 Jan;
71(10):2350-2354.
PMID: 34974569
Objective: To explore the spectrum of presentation, underlying monogenetic defects and outcome in very early onset inflammatory bowel disease (VEO-IBD). Method: The prospective, observational study was conducted at the Children's...
4.
Waheed N, Saeed A, Ijaz S, Fayyaz Z, Anjum M, Zahoor Y, et al.
J Pediatr Endocrinol Metab
. 2020 Jul;
33(9):1117-1123.
PMID: 32697758
Background PHKG2-related liver phosphorylase kinase deficiency is inherited in autosomal recessive pattern and is a rare type of liver glycogenosis. We demonstrated the clinical presentation and genetic determinants involved in...
5.
Zahoor M, Cheema H, Ijaz S, Fayyaz Z
Fetal Pediatr Pathol
. 2019 Oct;
39(5):430-440.
PMID: 31584309
Inborn errors of metabolism are inherited disorders that present in early childhood and are usually caused by monogenic recessive mutations in specific enzymes that metabolize dietary components. Distinct mutations are...
6.
Bilal H, Cheema H, Fayyaz Z, Saeed A, Batool Hamdani S
J Ayub Med Coll Abbottabad
. 2019 Sep;
31(3):368-371.
PMID: 31535508
Background: Objectives of the study were to determine the clinical spectrum of presentation and various modalities helpful in the diagnosis of liver glycogenosis short of genetic analysis. Methods: All patients...
7.
Waheed N, Cheema H, Saeed A, Alvi M, Fayyaz Z, Anjum N, et al.
J Ayub Med Coll Abbottabad
. 2019 Mar;
30(Suppl 1)(4):S673-S675.
PMID: 30838830
Over the past decade there is increased use of vitamin D supplementation because of its benefits on bone health. It is a fat-soluble vitamin and cannot be excreted from the...
8.
Cheema H, Malik H, Waheed N, Mushtaq I, Fayyaz Z, Anjum M
J Coll Physicians Surg Pak
. 2018 Apr;
28(5):406-408.
PMID: 29690976
Berardinelli-Seip congenital lipodystrophy (BSCL) syndrome is a rare genetic disorder caused by dysregulation of glycemic and lipid metabolism. We report five BSCL cases with typical clinical pictures and complications. These,...
9.
Waheed N, Cheema H, Suleman H, Mushtaq I, Fayyaz Z, Anjum N
J Coll Physicians Surg Pak
. 2018 Apr;
28(5):344-347.
PMID: 29690960
Objective: To differentiate between clinical and demographic spectrum, and outcome in hepatovenocaval syndrome (HVCS) and Budd-Chiari syndrome (BCS). Study Design: Descriptive study. Place And Duration Of Study: Division of Pediatric...
10.
Malik H, Cheema H, Fayyaz Z, Hashmi M, Parkash A, Waheed N, et al.
J Ayub Med Coll Abbottabad
. 2017 Jul;
28(3):518-522.
PMID: 28712226
Background: Spontaneous perforation of bile duct (SPBD) is a rare and often misdiagnosed entity. Though rare, it is the second most common surgical cause of jaundice in infants, after biliary...