Mohammad Hamid

Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency

Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian et al. · Matrix Biology · 2018 · 63 citations · Full text

Mendelian Disorder, Genetic Disorder, Lysyl Hydroxylase 3 +5

Magnesium, a drug of diverse use.

Mohammad Irfan Akhtar, Hameed Ullah, Mohammad Hamid · PubMed · 2011 · 34 citations

Molecular Pharmacology, Skeletal Muscle, Active Ingredient +13

Safety profile of fast-track extubation in pediatric congenital heart disease surgery patients in a tertiary care hospital of a developing country: An observational prospective study

MohammadIrfan Akhtar, Mohammad Hamid, Fauzia Minai et al. · Journal of Anaesthesiology Clinical Pharmacology · 2014 · 29 citations · Full text

Multicenter International Survey on the Clinical Practice of Ultra-Fast-Track Anesthesia with On-Table Extubation in Pediatric Congenital Cardiac Surgery

Mohammad Irfan Akhtar, Mona Momeni, Andrea Székely et al. · Journal of Cardiothoracic and Vascular Anesthesia · 2018 · 29 citations · Full text

Cardiac Anaesthesia, Cardiothoracic Surgery, Pediatric Heart Disease +14

Influence of glutathione S‐transferases (GSTM1, GSTT1, and GSTP1) genetic polymorphisms and smoking on susceptibility risk of chronic myeloid leukemia and treatment response

Golale Rostami, Dlnya Assad, Fatemeh Ghadyani et al. · Molecular Genetics & Genomic Medicine · 2019 · 28 citations · Full text