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Volumn 48, Issue 2, 2000, Pages 227-232

Further evidence for genetic heterogeneity in familial hemophagocytic lymphohistiocytosis (FHLH)

(7) Graham, Gail E a,c Graham, Lisa M a Bridge, Peter J a Maclaren, Linda D a Wolff, Johannes E A a,b Coppes, Max J a,b Egeler, R Maarten a,b

a UNIVERSITY OF CALGARY (Canada)

b UNIVERSITY OF CALGARY (Canada)

c ALBERTA CHILDREN'S HOSPITAL (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOSTEROID; CYCLOSPORIN A; METHOTREXATE;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BONE MARROW TRANSPLANTATION; CHILD; CHROMOSOME 10Q; CHROMOSOME 9Q; FEMALE; GENE LOCUS; GENE SEGREGATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; HEMOPHAGOCYTIC SYNDROME; HISTIOCYTOSIS; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; IMMUNOREGULATION; INFANT; MALE; PRIORITY JOURNAL;

EID: 0033930892 PISSN: 00313998 EISSN: None Source Type: Journal
DOI: 10.1203/00006450-200008000-00017 Document Type: Article

Times cited : (21)

References (19)

1
- 0029111779
- Medical progress: Langerhans cell histiocytosis
- (1995) J Pediatr , vol.127 , pp. 1-11
- Egeler, R.M.¹ D'Angio, G.J.²

2
- 0021150963
- Genetic analysis of familial erythrophagocytic lymphohistiocytosis
- (1984) Eur J Pediatr , vol.142 , pp. 248-252
- Gencik, A.¹ Signer, E.² Muller, H.J.³

3
- 85037960355
- Online Mendelian Inheritance in Man, OMIM(TM). Johns Hopkins University. Baltimore, MD MIM Number: 267700:12/20/99. World Wide Web
- (1999)

4
- 0033361023
- Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mapping
- (1999) Am J Hum Genet , vol.64 , pp. 165-171
- Ohadi, M.¹ Lalloz, M.R.A.² Sham, P.³ Zhao, J.⁴ Dearlove, A.M.⁵ Shiach, C.⁶ Kinsey, S.⁷ Rhodes, M.⁸ Layton, D.M.⁹

5
- 0033364525
- Linkage of familial hemophagocytic lymphohistiocytosis to 10q21-22 and evidence for heterogeneity
- (1999) Am J Hum Genet , vol.64 , pp. 172-179
- Dufourcq-Lagelouse, R.¹ Jabado, N.² Le Deist, F.³ Stephan, J.L.⁴ Souillet, G.⁵ Bruin, M.⁶ Vilmer, E.⁷ Schneider, M.⁸ Janka, G.⁹ Fischer, A.¹⁰ De Saint Basile, G.¹¹

6
- 0033520970
- Perforin gene defects in familial hemophagocytic lymphohistiocytosis
- (1999) Science , vol.286 , pp. 1957-1959
- Stepp, S.E.¹ Dufourcq-Lagelouse, R.² Le Deist, F.³ Bhawan, S.⁴ Certain, S.⁵ Mathew, P.A.⁶ Henter, J.I.⁷ Bennett, M.⁸ Fischer, A.⁹ De Saint Basile, G.¹⁰ Kumar, V.¹¹

7
- 0030014402
- Haemophagocytic lymphohistiocytosis associated with constitutional inversion of chromosome 9
- (1996) Br J Haematol , vol.93 , pp. 808-809
- Hasle, H.¹ Brandt, C.² Kerndrup, G.³ Kjeldsen, E.⁴ Sorensen, A.G.⁵

8
- 0026065540
- Diagnostic guidelines for hemophagocytic lymphohistiocytosis. The FHL Study Group of the Histiocyte Society
- (1991) Semin Oncol , vol.18 , pp. 29-33
- Henter, J.I.¹ Elinder, G.² Ost, A.³

9
- 0023258542
- DNA banking: The effects of Storage of blood and isolated DNA on the integrity of DNA
- (1987) Am J Med Genet , vol.27 , pp. 379-390
- Madisen, L.¹ Hoar, D.I.² Holroyd, C.D.³ Crisp, M.⁴ Hodes, M.E.⁵

10
- 0029988255
- A metric map of humans: 23,500 Loci in 850 bands
- (1996) Proc Natl Acad Sci USA , vol.93 , pp. 14771-14775
- Collins, A.¹ Frezal, J.² Teague, J.³ Morton, N.E.⁴

11
- 0026061971
- Incidence in Sweden and clinical features of familial hemophagocytic lymphohistiocytosis
- (1991) Acta Paediatr Scand , vol.80 , pp. 428-435
- Henter, J.I.¹ Elinder, G.² Soder, O.³ Ost, A.⁴

12
- 0028097417
- Hemophagocytic lymphohistiocytosis. Experience at two U.K. centres
- (1994) Br J Haematol , vol.88 , pp. 731-739
- Hirst, W.J.¹ Layton, D.M.² Singh, S.³ Mieli-Vergani, G.⁴ Chessells, J.M.⁵ Strobel, S.⁶ Pritchard, J.⁷

13
- 0029862128
- Characteristic immune abnormalities in hemophagocytic lymphohistiocytosis
- (1996) J Pediatr Hematol Oncol , vol.18 , pp. 340-345
- Egeler, R.M.¹ Shapiro, R.S.² Loechelt, B.³ Filipovich, A.H.⁴

14
- 0020578818
- Familial hemophagocytic lymphohistiocytosis
- (1983) Eur J Pediatr , vol.140 , pp. 221-229
- Janka, G.E.¹

15
- 0018860647
- Successful treatment of lymphohistiocytic reticulosis with phagocytosis with epipodophyllotoxin VP16-213
- (1980) Cancer , vol.45 , pp. 2516-2520
- Ambruso, D.R.¹ Hays, T.² Zwartjes, W.J.³ Tubergen, D.G.⁴ Favara, B.E.⁵

16
- 0030937079
- HLH-94: Treatment protocol for hemophagocytic lymphohistiocytosis
- (1997) Med Pediatr Oncol , vol.28 , pp. 342-347
- Henter, J.I.¹ Arico, M.² Egeler, R.M.³ Elinder, G.⁴ Favara, B.E.⁵ Filipovich, A.H.⁶ Gadner, H.⁷ Imashuku, S.⁸ Janka-Schaub, G.⁹ Komp, D.¹⁰ Ladisch, S.¹¹ Webb, D.¹²

17
- 0031971651
- Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafness
- (1998) Am J Hum Genet , vol.62 , pp. 1123-1128
- Moynihan, L.M.¹ Bundey, S.E.² Heath, D.³ Jones, E.L.⁴ McHale, D.P.⁵ Mueller, R.F.⁶ Markham, A.F.⁷ Lench, N.J.⁸

18
- 1642633543
- Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individuals
- (1998) Am J Hum Genet , vol.63 , pp. 506-516
- Makela-Bengs, P.¹ Jarvinen, N.² Vuopala, K.³ Suomalainen, A.⁴ Ignatius, J.⁵ Sipila, M.⁶ Herva, R.⁷ Palotie, A.⁸ Peltonen, L.⁹

19
- 0031926347
- Infection- and malignancy-associated hemophagocytic syndromes
- In: Egeler RM, D'Angio GJ (eds) Langerhans Cell Histiocytosis, Hematology/Oncology Clinics of North America. WB Saunders, Philadelphia
- (1998) , pp. 435-444
- Janka, G.¹ Imashuku, S.² Elinder, G.³ Schneider, M.⁴ Henter, J.I.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.