238 related articles for article (PubMed ID: 32259894)
1. Neurological symptoms of familial hemophagocytic lymphohistiocytosis type 2.
Wang J; Tuo H; Wu L; Wang X; Wang Z
J Integr Neurosci; 2020 Mar; 19(1):131-135. PubMed ID: 32259894
[TBL] [Abstract][Full Text] [Related]
2. Central nervous system involvement in a case of familial hemophagocytic lymphohistiocytosis with perforin mutation.
Akbayram S; Akgun C; Dogan M; Caksen H; Okur H; Oner AF
Genet Couns; 2011; 22(3):281-5. PubMed ID: 22029169
[TBL] [Abstract][Full Text] [Related]
3. A neurologic presentation of familial hemophagocytic lymphohistiocytosis which mimicked septic emboli to the brain.
Turtzo LC; Lin DD; Hartung H; Barker PB; Arceci R; Yohay K
J Child Neurol; 2007 Jul; 22(7):863-8. PubMed ID: 17715280
[TBL] [Abstract][Full Text] [Related]
4. Central nervous system involvement in hemophagocytic lymphohistiocytosis: a single-center experience.
Jovanovic A; Kuzmanovic M; Kravljanac R; Micic D; Jovic M; Gazikalovic S; Pasic S
Pediatr Neurol; 2014 Mar; 50(3):233-7. PubMed ID: 24332871
[TBL] [Abstract][Full Text] [Related]
5. Hemophagocytic lymphohistiocytosis with isolated central nervous system reactivation and optic nerve involvement.
Chong KW; Lee JH; Choong CT; Paeds MM; Chan DW; Fortier MV; Chan MY
J Child Neurol; 2012 Oct; 27(10):1336-9. PubMed ID: 22378674
[TBL] [Abstract][Full Text] [Related]
6. A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis.
Bordbar MR; Modarresi F; Farazi Fard MA; Dastsooz H; Shakib Azad N; Faghihi MA
BMC Med Genet; 2017 May; 18(1):49. PubMed ID: 28468610
[TBL] [Abstract][Full Text] [Related]
7. Adult-onset hemophagocytic lymphohistiocytosis type 2 presenting as a demyelinating disease.
Algahtani H; Absi A; Bassuni W; Shirah B
Mult Scler Relat Disord; 2018 Oct; 25():77-82. PubMed ID: 30053752
[TBL] [Abstract][Full Text] [Related]
8. Predominant Neurologic Manifestations Seen in a Patient With a Biallelic Perforin1 Mutation (PRF1; p.R225W).
Madkaikar M; Gupta M; Dixit A; Patil V
J Pediatr Hematol Oncol; 2017 Mar; 39(2):143-146. PubMed ID: 27271812
[TBL] [Abstract][Full Text] [Related]
9. A teenage boy with late onset hemophagocytic lymphohistiocytosis with predominant neurologic disease and perforin deficiency.
Beaty AD; Weller C; Levy B; Vogler C; Ferguson WS; Bicknese A; Knutsen AP
Pediatr Blood Cancer; 2008 May; 50(5):1070-2. PubMed ID: 18074390
[TBL] [Abstract][Full Text] [Related]
10. Perforin gene mutation in familial haemophagocytic lymphohistiocytosis: the first reported case from Hong Kong.
Chiang GP; Li CK; Lee V; Cheng FW; Leung AW; Imashuku S; Imamura T; Shing MM
Hong Kong Med J; 2014 Aug; 20(4):339-42. PubMed ID: 25104007
[TBL] [Abstract][Full Text] [Related]
11. Neuromyelitis optica, atypical hemophagocytic lymphohistiocytosis and heterozygous perforin A91V mutation.
Palterer B; Brugnolo F; Sieni E; Barilaro A; Parronchi P
J Neuroimmunol; 2017 Oct; 311():10-13. PubMed ID: 28863861
[TBL] [Abstract][Full Text] [Related]
12. Rare cause of Hemophagocytic Lymphohistiocytosis due to mutation in PRF1 and SH2D1A genes in two children - a case report with a review.
Sheth J; Patel A; Shah R; Bhavsar R; Trivedi S; Sheth F
BMC Pediatr; 2019 Mar; 19(1):73. PubMed ID: 30849948
[TBL] [Abstract][Full Text] [Related]
13. Case Report: Chronic inflammatory demyelinating polyradiculoneuropathy rather than hemophagocytic lymphohistiocytosis-the initial phenotype of PRF1 gene mutation.
Hu LY; Wan L; Wang QH; Shi XY; Meng Y; Yang XF; Yang G; Zou LP
Front Immunol; 2023; 14():1306338. PubMed ID: 38149249
[TBL] [Abstract][Full Text] [Related]
14. Previously undiagnosed fatal familial haemophagocytic lymphohistiocytosis in a 24-year-old woman.
Barmettler S; Nowak RJ; Parker T; Price C
BMJ Case Rep; 2016 Feb; 2016():. PubMed ID: 26903364
[TBL] [Abstract][Full Text] [Related]
15. Hemophagocytic lymphohistiocytosis with a hemizygous PRF1 c.674G>A mutation.
Xin X; Wang N; Zhang Y
Am J Med Sci; 2023 Nov; 366(5):387-394. PubMed ID: 37467895
[TBL] [Abstract][Full Text] [Related]
16. A Case of Familial Hemophagocytic Lymphohistiocytosis Type 4 With Involvement of the Central Nervous System Complicated With Infarct.
Ciraci S; Ozcan A; Ozdemir MM; Chiang SCC; Tesi B; Ozdemir AM; Karakukcu M; Patiroglu T; Acipayam C; Doganay S; Gumus H; Unal E
J Pediatr Hematol Oncol; 2017 Aug; 39(6):e321-e324. PubMed ID: 28692549
[TBL] [Abstract][Full Text] [Related]
17. Brain MRI imaging markers associated with death in children with central nervous system involvement of hemophagocytic lymphohistiocytosis.
Ma W; Zhou L; Li W; Li X; Huang Y; Gao S; Yu J; Fang Y; Xu Y
Eur Radiol; 2024 Feb; 34(2):873-884. PubMed ID: 37624411
[TBL] [Abstract][Full Text] [Related]
18. Perforin gene analaysis in an Iranian family with familial hemophagocytic lymphohistiocytosis.
Galehdari H; Mohammadi E; Andashti B; Naderi A; Molavi MA
Iran J Immunol; 2007 Jun; 4(2):122-6. PubMed ID: 17652853
[TBL] [Abstract][Full Text] [Related]
19. Hemophagocytic Lymphohistiocytosis Associated with Disseminated Nontuberculous Mycobacterial Infection in a Patient with Mesenteric Panniculitis.
Fujita Y; Matsumoto H; Asano T; Sato S; Yashiro-Furuya M; Matsuoka N; Temmoku J; Nakatani-Enomoto S; Kimura S; Hoshi K; Uematsu M; Watanabe H; Migita K
Tohoku J Exp Med; 2021 Feb; 253(2):151-157. PubMed ID: 33658450
[TBL] [Abstract][Full Text] [Related]
20. Neurological Abnormality Could be the First and Only Symptom of Familial Hemophagocytic Lymphohistiocytosis: Report of Two Families.
Zhao YZ; Cheng H; Ding CH; Ma HH; Han TL; Li JW; Wang D; Li ZG; Wang TY; Zhang R
Chin Med J (Engl); 2018 Dec; 131(24):3004-3006. PubMed ID: 30539918
[No Abstract] [Full Text] [Related]
[Next] [New Search]
