These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 35470934)

  • 21. Familial haemophagocytosis lymphohisticytosis type 3: A case report.
    Kamoun F; Hsairi M; Grandin V; Ben Ameur S; De Saint Basile G; Hachicha M
    Arch Pediatr; 2017 Jan; 24(1):33-35. PubMed ID: 27914778
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Detection of a novel gross deletion in the UNC13D gene ends the diagnostic odyssey for a family with familial hemophagocytic lymphohistiocytosis 3.
    Nagaraj CB; Brightman DS; Rea H; Wakefield E; Harkavy NVG; Dyer L; Zhang W
    BMC Pediatr; 2024 Jan; 24(1):34. PubMed ID: 38212754
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Novel deep intronic and missense UNC13D mutations in familial haemophagocytic lymphohistiocytosis type 3.
    Entesarian M; Chiang SC; Schlums H; Meeths M; Chan MY; Mya SN; Soh SY; Nordenskjöld M; Henter JI; Bryceson YT
    Br J Haematol; 2013 Aug; 162(3):415-8. PubMed ID: 23672263
    [No Abstract]   [Full Text] [Related]  

  • 24. Familial hemophagocytic lymphohistiocytosis in the neonate.
    Whaley BF
    Adv Neonatal Care; 2011 Apr; 11(2):101-7. PubMed ID: 21730897
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Fatal unexpected death due to familial hemophagocytic lymphohistiocytosis type 3.
    Mu J; Jin C; Chen Z; Li J; Lv B; Dong H
    Forensic Sci Med Pathol; 2018 Sep; 14(3):372-376. PubMed ID: 29754257
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Familial Hemophagocytic Lymphohistiocytosis Screening in Neonatal Sepsis.
    Kadi Ozan Z; Erduran E; Ceylaner S; Aslan Y; Bahadir A; Reis GP; Mutlu M
    J Pediatr Hematol Oncol; 2024 Aug; 46(6):e393-e401. PubMed ID: 38968556
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Retroviral
    Dettmer V; Bloom K; Gross M; Weissert K; Aichele P; Ehl S; Cathomen T
    Hum Gene Ther; 2019 Aug; 30(8):975-984. PubMed ID: 31032638
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Different Clinical Presentation of 3 Children With Familial Hemophagocytic Lymphohistiocytosis With 2 Novel Mutations.
    Akyol S; Ozcan A; Sekine T; Chiang SCC; Yilmaz E; Karakurkcu M; Patiroglu T; Bryceson Y; Unal E
    J Pediatr Hematol Oncol; 2020 Oct; 42(7):e627-e629. PubMed ID: 31651726
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Familial hemophagocytic lymphohistiocytosis.
    Herman TE; Siegel MJ
    J Perinatol; 2010 May; 30(5):363-5. PubMed ID: 20428180
    [No Abstract]   [Full Text] [Related]  

  • 30. Neonatal primary hemophagocytic lymphohistiocytosis in Turkish children.
    Gurgey A; Unal S; Okur H; Orhan D; Yurdakok M
    J Pediatr Hematol Oncol; 2008 Dec; 30(12):871-6. PubMed ID: 19131769
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Combined newborn screening for familial hemophagocytic lymphohistiocytosis and severe T- and B-cell immunodeficiencies.
    Borte S; Meeths M; Liebscher I; Krist K; Nordenskjöld M; Hammarström L; von Döbeln U; Henter JI; Bryceson YT
    J Allergy Clin Immunol; 2014 Jul; 134(1):226-8. PubMed ID: 24882743
    [No Abstract]   [Full Text] [Related]  

  • 32. Rotavirus-associated hemophagocytic lymphohistiocytosis (HLH) after hematopoietic stem cell transplantation for familial HLH.
    Park M; Yun YJ; Woo SI; Lee JW; Chung NG; Cho B
    Pediatr Int; 2015 Apr; 57(2):e77-80. PubMed ID: 25712613
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Novel mutations in the UNC13D gene carried by a Chinese neonate with hemophagocytic lymphohistiocytosis.
    Chen Y; Wang Z; Cheng Y; Tang Y
    Yonsei Med J; 2013 Jul; 54(4):1053-7. PubMed ID: 23709445
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Lentiviral Gene Therapy for Familial Hemophagocytic Lymphohistiocytosis Type 3, Caused by
    Takushi SE; Paik NY; Fedanov A; Prince C; Doering CB; Spencer HT; Chandrakasan S
    Hum Gene Ther; 2020 Jun; 31(11-12):626-638. PubMed ID: 32253931
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Novel STXBP2 mutation causing familial hemophagocytic lymphohistiocytosis.
    Jain R; Puliyel M; Moses PD; Sieni E
    Indian Pediatr; 2012 Jun; 49(6):488-90. PubMed ID: 22796692
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Alternative
    Galgano D; Soheili T; Voss M; Torralba-Raga L; Tesi B; Cichocki F; Andre I; Rettig J; Cavazzana M; Bryceson Y
    Front Immunol; 2020; 11():1154. PubMed ID: 32582217
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Hemophagocytic lymphohistiocytosis with Munc13-4 mutation: a cause of recurrent fatal hydrops fetalis.
    Bechara E; Dijoud F; de Saint Basile G; Bertrand Y; Pondarré C
    Pediatrics; 2011 Jul; 128(1):e251-4. PubMed ID: 21646258
    [TBL] [Abstract][Full Text] [Related]  

  • 38. COVID-19 Induced Hemophagocytic Lymphohistiocytosis in a Patient with Novel Homozygous UNC13D Gene Variant.
    Tekeli S; Erman B; Kurucu B; Tanir G; Aytekin C
    Klin Padiatr; 2023 Jul; 235(4):258-260. PubMed ID: 37493977
    [No Abstract]   [Full Text] [Related]  

  • 39. Rare coincidence of familial central core disease and hemophagocytic lymphohistiocytosis.
    Lee JS; Lim BC; Kim KJ; Hwang YS; Seong MW; Park SS; Park SH; Chae JH
    Pediatr Int; 2014 Dec; 56(6):e88-e91. PubMed ID: 25521991
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Fetal Splenomegaly: A Review.
    Moreira M; Brás R; Gonçalves D; Alencoão I; Inocêncio G; Rodrigues M; Braga J
    Ultrasound Q; 2018 Mar; 34(1):32-33. PubMed ID: 29194292
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.