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The many faces of peroxisomal disorders: Lessons from a large Arab cohort.
Alshenaifi, Jumanah; Ewida, Nour; Anazi, Shams; Shamseldin, Hanan E; Patel, Nisha; Maddirevula, Sateesh; Al-Sheddi, Tarfa; Alomar, Rana; Alobeid, Eman; Ibrahim, Niema; Hashem, Mais; Abdulwahab, Firdous; Jacob, Minnie; Alhashem, Amal; Alzaidan, Hamad I; Seidahmed, Mohammed Z; Alhashemi, Nadia; Rawashdeh, Rifaat; Eyaid, Wafaa; Al-Hassnan, Zuhair N; Rahbeeni, Zuhair; Alswaid, Abdulrahman; Hadid, Adnan; Qari, Alya; Mohammed, Dia A; El Khashab, Heba Y; Alfadhel, Majid; Abanemai, Mohammad; Sunbul, Rawda; Al Tala, Saeed; Alkhalifi, Salwa; Alkharfi, Turki; Abouelhoda, Mohamed; Monies, Dorota; Al Tassan, Nada; AlDubayan, Saud H; Kurdi, Wesam; Al-Owain, Mohammed; Dasouki, Majed J; Kentab, Amal Y; Atyani, Suha; Makhseed, Nawal; Faqeih, Eissa; Shaheen, Ranad; Alkuraya, Fowzan S.
Afiliación
  • Alshenaifi J; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Ewida N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Anazi S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Shamseldin HE; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Patel N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Maddirevula S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al-Sheddi T; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alomar R; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alobeid E; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Ibrahim N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Hashem M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Abdulwahab F; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Jacob M; The Newborn Screening and Biochemical Genetics Laboratory, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alhashem A; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Alzaidan HI; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Seidahmed MZ; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Alhashemi N; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Rawashdeh R; Department of Pediatrics, Security Forces Hospital, Riyadh, Saudi Arabia.
  • Eyaid W; Department of Pediatrics, Royal Hospital, Muscat, Oman.
  • Al-Hassnan ZN; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Rahbeeni Z; Medical Genetic Division, Department of Pediatrics, King Abdullah International Medical Research Centre, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Alswaid A; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Hadid A; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Qari A; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Mohammed DA; Medical Genetic Division, Department of Pediatrics, King Abdullah International Medical Research Centre, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • El Khashab HY; Department of Pediatrics College of Medicine and King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.
  • Alfadhel M; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Abanemai M; Department of Pediatrics, Makkah Maternity and Children's Hospital, Makkah, Saudi Arabia.
  • Sunbul R; Department of Pediatrics Dr. Sulimann AL Habib Medical Group, Riyadh, Saudi Arabia.
  • Al Tala S; Department of Pediatrics, Division of Pediatric Neurology Children Hospital, Ain Shams University, Cairo, Egypt.
  • Alkhalifi S; Medical Genetic Division, Department of Pediatrics, King Abdullah International Medical Research Centre, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Alkharfi T; Pediatrics Department, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Abouelhoda M; Pediatrics Medical Genetic Unit (PMGU), Pediatrics Department, Qatif Central Hospital, Qatif, Saudi Arabia.
  • Monies D; Armed Forces Hospital Southern Region, Pediatric Directorate and Genetic Unit Khamis Mushayt, Khamis Mushait, Saudi Arabia.
  • Al Tassan N; Maternity and Children's Hospital, Dammam, Saudi Arabia.
  • AlDubayan SH; Department of Pediatrics, Sanad Hospital, Riyadh, Saudi Arabia.
  • Kurdi W; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al-Owain M; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Dasouki MJ; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Kentab AY; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Atyani S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Makhseed N; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Faqeih E; Department of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Shaheen R; Division of Genetics, Brigham and Women's Hospital, Boston, Massachusetts.
  • Alkuraya FS; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
Clin Genet ; 95(2): 310-319, 2019 02.
Article en En | MEDLINE | ID: mdl-30561787
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trastorno Peroxisomal / Árabes Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Idioma: En Revista: Clin Genet Año: 2019 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trastorno Peroxisomal / Árabes Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Idioma: En Revista: Clin Genet Año: 2019 Tipo del documento: Article