Functional characterization of two RAB27A missense mutations found in Griscelli syndrome type 2 von Ohbayashi, Norihiko, Mamishi, Setareh, Ishibashi, Koutaro, Maruta, Yuto, Pourakbari, Babak, Tamizifar, Banafshe, Mohammadpour, Masoud, Fukuda, Mitsunori, Parvaneh, Nima

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Adenosine Deaminase (ADA) Deficiency: Report of Six New Cases and Reappraisal of Cutaneous Hypermelanosis as an Early Feature von Sharafian, Samin, Jacomelli, Gabriella, Tamizifar, Banafshe, Shahrooei, Mohammad, Parvaneh, Nima

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Analysis of RAB27A Gene in Griscelli Syndrome type 2: Novel Mutations Including a Deletion Hotspot von Mamishi, Setareh, Modarressi, Mohammad Hossein, Pourakbari, Babak, Tamizifar, Banafshe, Mahjoub, Fatemeh, Fahimzad, Alireza, Alyasin, Soheila, Bemanian, Mohamad Hassan, Hamidiyeh, Amir Ali, Fazlollahi, Mohammad Reza, Ashrafi, Mahmoud Reza, Isaeian, Anna, Khotaei, Ghamartaj, Yeganeh, Mehdi, Parvaneh, Nima

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Aggressive and Neglected Basal Cell Carcinoma von Asilian, Ali, Tamizifar, Banafshe

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Diffuse dermal melanocytosis in two patients with Sandhoff disease and mucopolysaccharidosis VI von Ashrafi, Mahmoud Reza, Tavasoli, Alireza, Shiva, Shadi, Parvaneh, Nima, Tamizifar, Banafshe

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Diffuse dermal melanocytosis in two patients with S andhoff disease and mucopolysaccharidosis VI von Ashrafi, Mahmoud Reza, Tavasoli, Alireza, Shiva, Shadi, Parvaneh, Nima, Tamizifar, Banafshe

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Characterization of 11 New Cases of Leukocyte Adhesion Deficiency Type 1 with Seven Novel Mutations in the ITGB2 Gene von Parvaneh, Nima, Mamishi, Setareh, Rezaei, Amir, Rezaei, Nima, Tamizifar, Banafshe, Parvaneh, Leila, Sherkat, Roya, Ghalehbaghi, Babak, Kashef, Sara, Chavoshzadeh, Zahra, Isaeian, Anna, Ashrafi, Farzaneh, Aghamohammadi, Asghar

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Aggressive and Neglected Basal Cell Carcinoma von Asilian, Ali, Tamizifar, Banafshe

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Paraffinoma and ulcer of the external genitalia after self-injection of nandrolone von Balighi, Kamran, Farsinejad, Khalil, Naraghi, Zahra S., Tamizifar, Banafshe

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Novel mutations of NP in two patients with purine nucleoside phosphorylase deficiency von Parvaneh, Nima, Teimourian, Shahram, Jacomelli, Gabriella, Badalzadeh, Mohsen, Bertelli, Matteo, Zakharova, Ekaterina, Tabatabaei, Parviz, Parvaneh, Leila, Pourakbari, Babak, Yeganeh, Mehdi, Tamizifar, Banafshe, Mamishi, Setareh, Micheli, Vanna

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Cutaneous granulomas in common variable immunodeficiency: case report and review of literature von Aghamohammadi, Asghar, Abolhassani, Hassan, Rezaei, Nima, Kalantari, Najmoddin, Tamizifar, Banafshe, Cheraghi, Taher, Parvaneh, Nima, Yeganeh, Mehdi, Moazzami, Kasra, Ebrahimi-Daryani, Naser, Anaraki, Mohammad Reza

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Adenosine Deaminase (ADA) Deficiency: Report of Six New Cases and Reappraisal of Cutaneous Hypermelanosis as an Early Feature von Sharafian, Samin, Jacomelli, Gabriella, Tamizifar, Banafshe, Shahrooei, Mohammad, Parvaneh, Nima

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Other Well-Defined Immunodeficiencies von Yeganeh, Mehdi, Gambineri, Eleonora, Abolmaali, Kamran, Tamizifar, Banafshe, Español, Teresa

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Novel mutations of NP in two patients with purine nucleoside phosphorylase deficiency von Parvaneh, Nima, Teimourian, Shahram, Jacomelli, Gabriella, Badalzadeh, Mohsen, Bertelli, Matteo, Zakharova, Ekaterina, Tabatabaei, Parviz, Parvaneh, Leila, Pourakbari, Babak, Yeganeh, Mehdi, Tamizifar, Banafshe, Mamishi, Setareh, Micheli, Vanna

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