Karamizadeh Z - Search Results

1

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. Among authors: karamizadeh z. 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

2

Isolated growth hormone deficiency in a patient with immunoglobulin class switch recombination deficiency.

Kashef S, Ghaedian MM, Rezaei N, Karamizadeh Z, Aghamohammadi A, Durandy A, Pan-Hammarstrom Q, Hammarstrom L. Kashef S, et al. Among authors: karamizadeh z. J Investig Allergol Clin Immunol. 2009;19(3):233-6. J Investig Allergol Clin Immunol. 2009. PMID: 19610268 Free article.

3

Bone mineral density in children wth systemic lupus erythematosus and juvenile rheumatoid arthritis.

Kashef S, Saki F, Karamizadeh Z, Kashef MA. Kashef S, et al. Among authors: karamizadeh z. Ann Saudi Med. 2007 Nov-Dec;27(6):427-31. doi: 10.5144/0256-4947.2007.427. Ann Saudi Med. 2007. PMID: 18059123 Free PMC article.

4

Juvenile paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation.

Saki F, Karamizadeh Z, Nasirabadi S, Mumm S, McAlister WH, Whyte MP. Saki F, et al. Among authors: karamizadeh z. J Bone Miner Res. 2013 Jun;28(6):1501-8. doi: 10.1002/jbmr.1868. J Bone Miner Res. 2013. PMID: 23322328 Free PMC article.

5

The role of insulin like growth factor (IGF)-1 and IGF-binding protein-3 in diagnosis of Growth Hormone Deficiency in short stature children.

Haghshenas Z, Sotoudeh K, Karamifar H, Karamizadeh Z, Amirhakimi G. Haghshenas Z, et al. Among authors: karamizadeh z. Indian J Pediatr. 2009 Jul;76(7):699-703. doi: 10.1007/s12098-009-0115-0. Epub 2009 Apr 16. Indian J Pediatr. 2009. PMID: 19381505

6

A new mutation of Fanconi-Bickel syndrome with liver failure and pseudotumour cerebri.

Karamizadeh Z, Saki F, Imanieh MH, Zahmatkeshan M, Fardaee M. Karamizadeh Z, et al. J Genet. 2012;91(3):359-61. doi: 10.1007/s12041-012-0198-7. J Genet. 2012. PMID: 23271022 No abstract available.

7

Bruck syndrome - a rare syndrome of bone fragility and joint contracture and novel homozygous FKBP10 mutation.

Moravej H, Karamifar H, Karamizadeh Z, Amirhakimi G, Atashi S, Nasirabadi S. Moravej H, et al. Among authors: karamizadeh z. Endokrynol Pol. 2015;66(2):170-4. doi: 10.5603/EP.2015.0024. Endokrynol Pol. 2015. PMID: 25931047 Free article. Review.

8

Effect of Growth Hormone treatment on Height Velocity of Children with Pycnodysotosis.

Karamizadeh Z Md, Ilkhanipoor H Md, Bagheri F Md. Karamizadeh Z Md, et al. Iran J Pediatr. 2014 Apr;24(2):161-5. Iran J Pediatr. 2014. PMID: 25535534 Free PMC article.

9

Effect of pubertal suppression on linear growth and body mass index; a two-year follow-up in girls with genetic short stature and rapidly progressive puberty.

Karamizadeh Z, Amirhakimi A, Amirhakimi G. Karamizadeh Z, et al. Iran J Pediatr. 2014 Jun;24(3):293-9. Iran J Pediatr. 2014. PMID: 25562023 Free PMC article.

10

Combined use of growth hormone and gonadotropin-releasing hormone analogue in short normal adolescent girls: a survey from Iran.

Karamizadeh Z, Kashef MA, Jalaeian H, Namazee N. Karamizadeh Z, et al. Kaohsiung J Med Sci. 2006 Apr;22(4):161-5. doi: 10.1016/S1607-551X(09)70301-8. Kaohsiung J Med Sci. 2006. PMID: 16679296 Free article.

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