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Did you mean m karamzadeh (12 results)?
Evaluation of congenital hypothyroidism in fars province, iran.
Karamizadeh Z, Saneifard H, Amirhakimi G, Karamifar H, Alavi M. Karamizadeh Z, et al. Iran J Pediatr. 2012 Mar;22(1):107-12. Iran J Pediatr. 2012. PMID: 23056868 Free PMC article.
The newborns with TSH 5mIU/L were recalled for measurement of serumT(4) and TSH in venous blood samples FINDINGS: Of 127 recalled subjects, 43 were confirmed to be hypothyroid, showing a prevalence of 1:1465 with F:M ratio of 1.05:1. The most common clinical and radiologic …
The newborns with TSH 5mIU/L were recalled for measurement of serumT(4) and TSH in venous blood samples FINDINGS: Of 127 recalled subjects, …
The side effects of gonadotropin releasing hormone analog (diphereline) in treatment of idiopathic central precocious puberty.
Karamizadeh Z, Tabebordbar M, Saki F, Karamifar H, Amirhakimi G. Karamizadeh Z, et al. Acta Med Iran. 2013;51(1):41-6. Acta Med Iran. 2013. PMID: 23456583 Free article.
Waist circumference, weight and BMI were 69.3 cm, 37.21 kg, and 19.13 kg/cm(2) before therapy and 72.25 cm, 40.11 kg, and 19.54 kg/m(2) 6 months after therapy respectively. Mean systolic and diastolic blood pressure of the patients before therapy was 96.83 mmHg, 66mmHg and …
Waist circumference, weight and BMI were 69.3 cm, 37.21 kg, and 19.13 kg/cm(2) before therapy and 72.25 cm, 40.11 kg, and 19.54 kg/m( …
Novel AICDA mutation in a case of autosomal recessive hyper-IgM syndrome, growth hormone deficiency and autoimmunity.
Fazel A, Kashef S, Aleyasin S, Harsini S, Karamizadeh Z, Zoghi S, Flores SK, Boztug K, Rezaei N. Fazel A, et al. Allergol Immunopathol (Madr). 2017 Jan-Feb;45(1):82-86. doi: 10.1016/j.aller.2016.08.005. Epub 2016 Oct 24. Allergol Immunopathol (Madr). 2017. PMID: 27789066
BACKGROUND: The Hyper-immunoglobulin M syndromes (HIGM) are a heterogeneous group of genetic disorders, which have been rarely reported to be associated with growth hormone deficiency (GHD). ...
BACKGROUND: The Hyper-immunoglobulin M syndromes (HIGM) are a heterogeneous group of genetic disorders, which have been rarely report …