Search Results - "Nasirabadi, Shiva"

Quality of life among Iranian patients with beta-thalassemia major using the SF-36 questionnaire by Haghpanah, Sezaneh, Nasirabadi, Shiva, Ghaffarpasand, Fariborz, Karami, Rahmatollah, Mahmoodi, Mojtaba, Parand, Shirin, Karimi, Mehran

“…CONTEXT AND OBJECTIVE Patients with beta-thalassemia major (β-TM) experience physical, psychological and social problems that lead to decreased quality of life…”
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Juvenile Paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation by Saki, Forough, Karamizadeh, Zohreh, Nasirabadi, Shiva, Mumm, Steven, McAlister, William H, Whyte, Michael P

“…ABSTRACT Juvenile Paget's disease (JPD) is a rare heritable osteopathy characterized biochemically by markedly increased serum alkaline phosphatase (ALP)…”
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Sociocultural challenges of beta-thalassaemia major birth in carriers of beta-thalassaemia in Iran by Haghpanah, Sezaneh, Nasirabadi, Shiva, Rahimi, Nazila, Faramarzi, Hossein, Karimi, Mehran

“…Despite premarital screening, prenatal diagnosis and the option for voluntary termination of pregnancy, some Iranian couples continue a pregnancy with a fetus…”
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The impact of renin–angiotensin system, angiotensin І converting enzyme (insertion/deletion), and angiotensin ІІ type 1 receptor (A1166C) polymorphisms on breast cancer survival in Iran by Namazi, Soha, Daneshian, Arghavan, Mohammadianpanah, Mohammad, Jafari, Peyman, Ardeshir-Rouhani-Fard, Shirin, Nasirabadi, Shiva

“…Several proteins of renin–angiotensin system (RAS) have been implicated in the process of growth promotion or inhibition of breast tissue and cancer cells…”
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Bruck syndrome - a rare syndrome of bone fragility and joint contracture and novel homozygous FKBP10 mutation by Moravej, Hossein, Karamifar, Hamdollah, Karamizadeh, Zohreh, Amirhakimi, Gholamhossein, Atashi, Sepideh, Nasirabadi, Shiva

“…Bruck syndrome is an autosomal recessive syndrome consisting of bone fragility and congenital joint contractures. According to the genotype, it has been…”
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A Classic Case of Maple Syrup Urine Disease and a Novel Mutation in the BCKDHA Gene by Alieh Mirzaee, Narges Pishva, Zohreh Karamizadeh, Jurgen Kohlhase, Shahnaz Purarian, Fariba Hemmati, Mostajab Razavi, Shiva Nasirabadi

“…Background: Maple syrup urine disease (MSUD) is an inherited branched-chain amino acid metabolic disorder caused by the deficiency in the branched-chain…”
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Zespół Brucka — rzadki zespół charakteryzujący się kruchością kości, przykurczami stawowymi i nowoodkrytą homozygotyczną mutacją FKBP10 by Moravej, Hossein, Karamifar, Hamdollah, Karamizadeh, Zohreh, Amirhakimi, Gholamhossein, Atashi, Sepideh, Nasirabadi, Shiva

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