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Items: 1 to 20 of 51

1.

Type 2 familial hemophagocytic lymphohistiocytosis in half brothers: A case report.

Liu C, Li M, Wu X, Yao X, Zhao L.

Medicine (Baltimore). 2018 Jul;97(30):e11577. doi: 10.1097/MD.0000000000011577.

2.

Low-Frequency Sensorineural Hearing Loss in Familial Hemophagocytic Lymphohistiocytosis Type 5.

Bezdjian A, Bruijnzeel H, Pagel J, Daniel SJ, Thomeer HGXM.

Ann Otol Rhinol Laryngol. 2018 Jun;127(6):409-413. doi: 10.1177/0003489418771714.

PMID:
29776323
3.

Is There Any Potential of FDG PET/CT in Monitoring Disease Activity in Familial Hemophagocytic Lymphohistiocytosis?

Tang Y, Tan H, Hu S.

Clin Nucl Med. 2018 Apr;43(4):296-298. doi: 10.1097/RLU.0000000000002008.

PMID:
29465491
4.

Young Man Battles For His Life Against Rare Autoimmune Disease.

Calandra R.

Manag Care. 2017 Oct;26(10):19-20.

5.

Finding a Balance between Protection and Pathology: The Dual Role of Perforin in Human Disease.

Willenbring RC, Johnson AJ.

Int J Mol Sci. 2017 Jul 25;18(8). pii: E1608. doi: 10.3390/ijms18081608. Review.

6.

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. doi: 10.1097/MPH.0000000000000886.

PMID:
28692549
7.

Germline heterozygous variants in genes associated with familial hemophagocytic lymphohistiocytosis as a cause of increased bleeding.

Fager Ferrari M, Leinoe E, Rossing M, Norström E, Strandberg K, Steen Sejersen T, Qvortrup K, Zetterberg E.

Platelets. 2018 Jan;29(1):56-64. doi: 10.1080/09537104.2017.1293808. Epub 2017 Apr 11.

PMID:
28399723
8.

A Newborn With Familial Hemophagocytic Lymphohistiocytosis Complicated With Transfusion Associated Graft Versus Host Disease.

Ozdemir A, Gunes T, Chiang SCC, Unal E.

J Pediatr Hematol Oncol. 2017 Aug;39(6):e309-e311. doi: 10.1097/MPH.0000000000000777.

PMID:
28328614
9.

Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G.

Kim MS, Cho YU, Jang S, Seo EJ, Im HJ, Park CJ.

Ann Lab Med. 2017 Mar;37(2):162-165. doi: 10.3343/alm.2017.37.2.162. No abstract available.

10.

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. doi: 10.1016/j.arcped.2016.10.021. Epub 2016 Nov 30.

PMID:
27914778
11.

A CD57+ CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients.

Hori M, Yasumi T, Shimodera S, Shibata H, Hiejima E, Oda H, Izawa K, Kawai T, Ishimura M, Nakano N, Shirakawa R, Nishikomori R, Takada H, Morita S, Horiuchi H, Ohara O, Ishii E, Heike T.

J Clin Immunol. 2017 Jan;37(1):92-99. doi: 10.1007/s10875-016-0357-3. Epub 2016 Nov 28.

PMID:
27896523
12.

Usual and Unusual Manifestations of Familial Hemophagocytic Lymphohistiocytosis and Langerhans Cell Histiocytosis.

Erker C, Harker-Murray P, Talano JA.

Pediatr Clin North Am. 2017 Feb;64(1):91-109. doi: 10.1016/j.pcl.2016.08.006. Review.

PMID:
27894453
13.

Successful treatment of recurrent CNS disease post-bone marrow transplant in children with familial hemophagocytic lymphohistiocytosis.

Bock AM, LeVeque M, Camitta B, Talano JA.

Pediatr Blood Cancer. 2016 Dec;63(12):2154-2158. doi: 10.1002/pbc.26175. Epub 2016 Aug 27.

PMID:
27565627
14.

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. doi: 10.1097/MPH.0000000000000597.

PMID:
27271812
15.

Impairment of Immune Function in Children with Familial Hemophagocytic Lymphohistiocytosis.

Popko K, Jasińska J, Górska E, Demkow U, Balwierz W, Maciejka-Kembłowska L, Badowska W, Wachowiak J, Drabko K, Malinowska I.

Adv Exp Med Biol. 2016;912:21-31. doi: 10.1007/5584_2016_210.

PMID:
26987330
16.

IL-2 consumption by highly activated CD8 T cells induces regulatory T-cell dysfunction in patients with hemophagocytic lymphohistiocytosis.

Humblet-Baron S, Franckaert D, Dooley J, Bornschein S, Cauwe B, Schönefeldt S, Bossuyt X, Matthys P, Baron F, Wouters C, Liston A.

J Allergy Clin Immunol. 2016 Jul;138(1):200-209.e8. doi: 10.1016/j.jaci.2015.12.1314. Epub 2016 Mar 4.

17.

Search for the potential "second-hit" mechanism underlying the onset of familial hemophagocytic lymphohistiocytosis type 2 by whole-exome sequencing analysis.

Gao L, Dang X, Huang L, Zhu L, Fang M, Zhang J, Xu X, Zhu L, Li T, Zhao L, Wei J, Zhou J.

Transl Res. 2016 Apr;170:26-39. doi: 10.1016/j.trsl.2015.12.004. Epub 2015 Dec 15.

PMID:
26739415
18.

A Novel Syntaxin 11 Gene (STX11) Mutation c.650T>C, p.Leu217Pro, in a Korean Child With Familial Hemophagocytic Lymphohistiocytosis.

Sultanova AK, Kim SK, Lee JW, Jang PS, Chung NG, Cho B, Park J, Kim Y, Kim M.

Ann Lab Med. 2016 Mar;36(2):170-3. doi: 10.3343/alm.2016.36.2.170.

19.

ST2 contributes to T-cell hyperactivation and fatal hemophagocytic lymphohistiocytosis in mice.

Rood JE, Rao S, Paessler M, Kreiger PA, Chu N, Stelekati E, Wherry EJ, Behrens EM.

Blood. 2016 Jan 28;127(4):426-35. doi: 10.1182/blood-2015-07-659813. Epub 2015 Oct 30.

20.

The Role of Hematopoietic Stem Cell Transplantation in Treatment of Hemophagocytic Lymphohistiocytosis.

Nikiforow S.

Hematol Oncol Clin North Am. 2015 Oct;29(5):943-59. doi: 10.1016/j.hoc.2015.06.011. Review.

PMID:
26461153

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