Zoekresultaten - "Omenn syndrome"

A case report of Omenn syndrome in siblings door Agnieszka Berendt, Monika Wójtowicz-Marzec, Monika Dobrowolska, Anna Kwaśniewska

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A case report of Omenn syndrome in siblings door Agnieszka Berendt, Monika Wójtowicz-Marzec, Monika Dobrowolska, Anna Kwaśniewska

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Desmoglein-1 Deficiency Mimicking Omenn Syndrome door Meltem Comert, Tugba Guler, Ayca Ceylan, İlknur Kulhas Celik, Pinar Karabagli, Tulin Cora, Hasibe Artac

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Omenn syndrome: a case report and review of literature door Chia-Chi Hsu, Julia Yu-Yun Lee, Sheau-Chiou Chao

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Molecular analysis of T^-B^-NK⁺severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia door Al-Kayal Fadi, Al-Saud Bandar, Al-Dhekri Hasan, Arnaout Rand, Al-Muhsen Saleh, Al-Ghonaium Abdulaziz, Alsmadi Osama, Al-Saud Haya, Al-Mousa Hamoud

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Gilbert Omenn and his syndrome door Ahmad Al Aboud, Khalid Al Aboud

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The Value of Family History in Diagnosing Primary Immunodeficiency Disorders door Mohamed A. Hendaus, Ahmad Alhammadi, Mehdi M. Adeli, Fawzia Al-Yafei

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Neonatal erythroderma: Diagnostic and therapeutic challenges door Sandipan Dhar, Raghubir Banerjee, Rajib Malakar

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Comèl-Netherton syndrome - case report door Izabela Błażewicz, Alicja Rustowska, Aleksandra Wilkowska, Roman J. Nowicki

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Inborn Errors of Immunity With Fetal or Perinatal Clinical Manifestations door Magda Carneiro-Sampaio, Adriana Almeida de Jesus, Silvia Yumi Bando, Carlos Alberto Moreira-Filho

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Novel mutatıons and diverse clinical phenotypes in recombınase-activating gene 1 deficiency door Kutukculer Necil, Gulez Nesrin, Karaca Neslihan, Aksu Guzide, Berdeli Afig

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