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Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases.
Sadeghi, Payman; Esslami, Golnaz Ghazizadeh; Rokni-Zadeh, Hassan; Changi-Ashtiani, Majid; Mohsenipour, Reihaneh.
Affiliation
  • Sadeghi P; Children's Medical Center, Pediatrics Center of Excellence, Tehran, Iran.
  • Esslami GG; Department of Pediatrics, Tehran University of Medical Sciences, Tehran, Iran.
  • Rokni-Zadeh H; Pediatric Rheumatology Society of Iran, Tehran, Iran.
  • Changi-Ashtiani M; Department of Emergency, Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
  • Mohsenipour R; Departments of Newborn Nursery, Neonates and Pediatrics, Ziaeian Hospital, Tehran University of Medical Sciences, Tehran, Iran.
BMC Pediatr ; 22(1): 667, 2022 11 19.
Article in En | MEDLINE | ID: mdl-36401200
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphohistiocytosis, Hemophagocytic Type of study: Diagnostic_studies / Guideline Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: BMC Pediatr Journal subject: PEDIATRIA Year: 2022 Document type: Article Affiliation country: Irán Country of publication: Reino Unido
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphohistiocytosis, Hemophagocytic Type of study: Diagnostic_studies / Guideline Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: BMC Pediatr Journal subject: PEDIATRIA Year: 2022 Document type: Article Affiliation country: Irán Country of publication: Reino Unido