Whole-Exome Sequencing in Idiopathic Short Stature: Rare Mutations Affecting Growth von Noorian, Shahab, Khonsari, Nami Mohammadian, Savad, Shahram, Hakak-Zargar, Benyamin, Voth, Tessa, Kabir, Koroush

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The Role of Thyroid Function Tests in Diagnosing Allan-herndon-dudley Syndrome Revisited: A Novel Iran-based Mutation von Noorian, Shahab, Hamzehlou, Sepideh, Rabbani, Ali, Sotoudeh, Arya, Pour Rostami, Kioumars, Savad, Shahram

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Late infantile form of multiple sulfatase deficiency von Mohammadian Khonsari, Nami, Hakak-Zargar, Benyamin, Voth, Tessa, Noorian, Shahab

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A Family With Novel X-Linked Recessive Homozygous Mutation in ANOS1 (c.628_629 del, p.1210fs∗) in Kallmann Syndrome Associated Unilateral Ptosis: Case Report and Literature Review... von Noorian, Shahab, Savad, Shahram, Khavandegar, Armin, Jamee, Mahnaz

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Dizygotic Twins Concordant for Down Syndrome: Implication for Establishing a National Birth Defect Registry in Iran von Savad, Shahram, Hamzehlou, Sepideh, Ghaffourian Abadi, Jila, Modarressi, Mohammad Hossein, Noorian, Shahab

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Familial hypercholesterolemia in an Iranian family due to a mutation in the APOE gene (first case report) von Noorian, Shahab, Razmandeh, Rezvan, Jazayeri, Roshanak

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Efficacy of teplizumab for treatment of type 1 diabetes: A meta‐analysis of randomized controlled trials von Heidari, Ehsan, Shafiee, Arman, Noorian, Shahab, Rafiei, Mohammad Ali, Abbasi, Mohammad, Amini, Mohammad Javad, Safari, Omid, Aghamahdi, Fatemeh, Bakhtiyari, Mahmood

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Associated factors to insulin adherence in type 1 diabetes in Tehran and Karaj, Iran von Fayyaz, Farimah, Aghamahdi, Fatemeh, Noorian, Shahab, Tabatabaei-Malazy, Ozra, Qorbani, Mostafa

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Compound Heterozygous Mutations Presented with Quadriparesis and Menopause. A Case Report von Noorian, Shahab, Mohammadpoor Nami, Sahar, Nouri Ghonbalani, Zahra, Mohammadian Khonsari, Nami

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GCK Mutation in a Child with Maturity Onset Diabetes of the Young, Type 2 von Noorian, Shahab, Sayarifard, Fatemeh, Farhadi, Elham, Barbetti, Fabrizio, Rezaei, Nima

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Reliability of pubertal self assessment method: an Iranian study von Rabbani, Ali, Noorian, Shahab, Fallah, Javad S, Setoudeh, Arya, Sayarifard, Fatemeh, Abbasi, Farzaneh

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Familial hypercholesterolemia in an Iranian family due to a mutation in the APOE gene (first case report) von Noorian, Shahab, Razmandeh, Rezvan, Jazayeri, Roshanak

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A novel missense mutation of the HGD gene causes Alkaptonuria von Noorian, Shahab, Dehghan Banadaki, Bahareh, Sotoudeh, Arya, Savad, Shahram, Modarressi, Mohammad Hossein

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A Family With Novel X-Linked Recessive Homozygous Mutation in ANOS1 (c.628_629 del, p.1210fs∗) in Kallmann Syndrome Associated Unilateral Ptosis: Case Report and Literature Review... von Noorian, Shahab, Savad, Shahram, Khavandegar, Armin, Jamee, Mahnaz

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GCK Mutation in a Child with Maturity Onset Diabetes of the Young, Type 2 von Noorian, Shahab, Sayarifard, Fatemeh, Farhadi, Elham, Barbetti, Fabrizio, Rezaei, Nima

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