Hasil Pencarian - Asieh Mosallanejad

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  1. 1
    3‐Hydroxyisobutyryl‐CoA hydrolase deficiency in an infant with developmental delay and high anion gap acidosis

    3‐Hydroxyisobutyryl‐CoA hydrolase deficiency in an infant with developmental delay and high anion gap acidosis oleh Hedyeh Saneifard, Asieh Mosallanejad, Aida Fallahzadeh, Ali Sheikhy

    Diterbitkan 2021-07-01
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  2. 2
    A Rare Case of Ovarian Hyperstimulation Syndrome in a Preterm Infant

    A Rare Case of Ovarian Hyperstimulation Syndrome in a Preterm Infant oleh Asieh Mosallanejad, Shahrzad Tabatabai, Marjan Shakiba, Mohammad Reza Alaei, Hedieh Saneifard

    Diterbitkan 2016-11-01
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  3. 3
    Proptosis, Micrognathia, Low Set Ear and Chest Deformity in a Patient with Extra Marker Chromosome 22

    Proptosis, Micrognathia, Low Set Ear and Chest Deformity in a Patient with Extra Marker Chromosome 22 oleh Asieh Mosallanejad, Fatemeh Sayarifard, Sima Hosseinverdi, Farzaneh Abbasi, Hosein Shabni Mirzaee, Nima Rezaei

    Diterbitkan 2015-10-01
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  4. 4
    Navigating ethical dilemmas in complementary and alternative medicine: a narrative review

    Navigating ethical dilemmas in complementary and alternative medicine: a narrative review oleh Mohammad Sadegh Adel Mehraban, Asieh Mosallanejad, Mehdi Mohammadi, Ozra Tabatabaei Malazy, Bagher Larijani

    Diterbitkan 2024-04-01
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  5. 5
    Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report

    Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report oleh Tahereh Ashraf Ganjooei, Zanbagh Pirastehfar, Asieh Mosallanejad, Masoomeh Raoufi, Noushin Afshar Moghaddam, Mozhgan Hashemieh

    Diterbitkan 2022-07-01
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  6. 6
    Clinical presentation and molecular genetics of Iranian patients with Niemann-pick type C disease and report of 6 NPC1 gene novel variants: A case series

    Clinical presentation and molecular genetics of Iranian patients with Niemann-pick type C disease and report of 6 NPC1 gene novel variants: A case series oleh Hedyeh Saneifard, Marjan Shakiba, Mohammadreza Alaei, Asieh Mosallanejad, Shirin Ghanefard, Mehrdad Yasaei, Kimia Karimi Toudeshki

    Diterbitkan 2024-09-01
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  7. 7
    Expanded inherited metabolic diseases screening by tandem mass spectrophotometry: The first report from Iran

    Expanded inherited metabolic diseases screening by tandem mass spectrophotometry: The first report from Iran oleh Marjan Shakiba, Mehrdad Yasaei, Hedyeh Saneifard, Asieh Mosallanejad, Mohammad Reza Alaei, Farzad Kobarfard, Marjan Esfahanizadeh, Narges Anousheh

    Diterbitkan 2024-09-01
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  8. 8
    Vitamin D Deficiency in Chronic Idiopathic Urticaria

    Vitamin D Deficiency in Chronic Idiopathic Urticaria oleh Masoud Movahedi, Marzieh Tavakol, Armin Hirbod-Mobarakeh, Mohammad Gharagozlou, Asghar Aghamohammadi, Zahra Tavakol, Kaveh Momenzadeh, Mohammad Nabavi, Abbas Dabbaghzade, Asieh Mosallanejad, Nima Rezaei

    Diterbitkan 2015-04-01
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