खोज परिणाम - Fatemeh Saffari

  • प्रदर्शित 1 - 5 परिणाम 5
परिणाम को परिष्कृत करें
  1. 1
    कवर छवि

    Treatment of Hypertension in a Child With 11Beta-Hydroxylase Deficiency: A Case Report द्वारा Fatemeh Saffari, Banafsheh Arad

    प्रकाशित 2022
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  2. 2
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    Novel Homozygous Nonsense Mutation in the LRP5 Gene in Two Siblings with Osteoporosis-pseudoglioma Syndrome द्वारा Abolfazl Heidari, Ali Homaei, Fatemeh Saffari

    प्रकाशित 2023
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  3. 3
    कवर छवि

    Identification of a Novel Mutation in an Iranian Family With 17-β Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Series द्वारा Abolfazl Heidari, Ali Homaei, Fatemeh Saffari

    प्रकाशित 2022
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  4. 4
    कवर छवि

    Causes of Precocious Puberty in Children Referred to an Endocrine Clinic in Qazvin City, Iran From 2006 to 2018 द्वारा Fatemeh Saffari, Roghayeh Golmohammadi, Ali Homaei

    प्रकाशित 2021
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  5. 5
    कवर छवि

    Prevalence of Sensorineural Hearing Loss in Patients with Congenital Hypothyroidism in Qazvin, Iran (2015) द्वारा Fatemeh Saffari, Mohammad Hassan Nikpendar, Neda Esmailzadehha, Sonia Oveisi, Ali Homaei, Shabnam Jalilolghadr

    प्रकाशित 2018
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    में बचाया:

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