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 *

176 related articles for article (PubMed ID: 1512605)

  • 1. McLeod syndrome: a distinct form of neuroacanthocytosis. Report of two cases and literature review with emphasis on neuromuscular manifestations.
    Witt TN; Danek A; Reiter M; Heim MU; Dirschinger J; Olsen EG
    J Neurol; 1992 Jul; 239(6):302-6. PubMed ID: 1512605
    [TBL] [Abstract][Full Text] [Related]  

  • 2. McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement.
    Jung HH; Hergersberg M; Vogt M; Pahnke J; Treyer V; Röthlisberger B; Kollias SS; Russo D; Frey BM
    Transfusion; 2003 Jul; 43(7):928-38. PubMed ID: 12823753
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A case of McLeod syndrome with unusually severe myopathy.
    Kawakami T; Takiyama Y; Sakoe K; Ogawa T; Yoshioka T; Nishizawa M; Reid ME; Kobayashi O; Nonaka I; Nakano I
    J Neurol Sci; 1999 Jun; 166(1):36-9. PubMed ID: 10465497
    [TBL] [Abstract][Full Text] [Related]  

  • 4. McLeod myopathy revisited: more neurogenic and less benign.
    Hewer E; Danek A; Schoser BG; Miranda M; Reichard R; Castiglioni C; Oechsner M; Goebel HH; Heppner FL; Jung HH
    Brain; 2007 Dec; 130(Pt 12):3285-96. PubMed ID: 18055495
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neuroacanthocytosis syndromes.
    Jung HH; Danek A; Walker RH
    Orphanet J Rare Dis; 2011 Oct; 6():68. PubMed ID: 22027213
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Kell, Kx and the McLeod syndrome.
    Redman CM; Russo D; Lee S
    Baillieres Best Pract Res Clin Haematol; 1999 Dec; 12(4):621-35. PubMed ID: 10895256
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a family.
    Malandrini A; Fabrizi GM; Truschi F; Di Pietro G; Moschini F; Bartalucci P; Berti G; Salvadori C; Bucalossi A; Guazzi G
    J Neurol Sci; 1994 Jun; 124(1):89-94. PubMed ID: 7931427
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hereditary acanthocytosis associated with the McLeod phenotype of the Kell blood group system.
    Symmans WA; Shepherd CS; Marsh WL; Oyen R; Shohet SB; Linehan BJ
    Br J Haematol; 1979 Aug; 42(4):575-83. PubMed ID: 476009
    [TBL] [Abstract][Full Text] [Related]  

  • 9. McLeod syndrome resulting from a novel XK mutation.
    Singleton BK; Green CA; Renaud S; Fuhr P; Poole J; Daniels GL
    Br J Haematol; 2003 Aug; 122(4):682-5. PubMed ID: 12899725
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An individual with McLeod syndrome and the Kell blood group antigen K(K1).
    Marsh WL; Schnipper EF; Johnson CL; Mueller KA; Schwartz SA
    Transfusion; 1983; 23(4):336-8. PubMed ID: 6879675
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel point mutation in the McLeod syndrome gene in neuroacanthocytosis.
    Ho MF; Chalmers RM; Davis MB; Harding AE; Monaco AP
    Ann Neurol; 1996 May; 39(5):672-5. PubMed ID: 8619554
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Benign X-linked myopathy with acanthocytes (McLeod syndrome). Its relationship to X-linked muscular dystrophy.
    Swash M; Schwartz MS; Carter ND; Heath R; Leak M; Rogers KL
    Brain; 1983 Sep; 106 (Pt 3)():717-33. PubMed ID: 6685553
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Malignant McLeod myopathy.
    Jung HH; Brandner S
    Muscle Nerve; 2002 Sep; 26(3):424-7. PubMed ID: 12210375
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel XK gene mutation in a Taiwanese family with McLeod syndrome.
    Chen PY; Lai SC; Yang CC; Lee MJ; Chiu YH; Yan SH; Lu CS; Yeh TH
    J Neurol Sci; 2014 May; 340(1-2):221-4. PubMed ID: 24635891
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Transfusion support for a patient with McLeod phenotype without chronic granulomatous disease and with antibodies to Kx and Km.
    Bansal I; Jeon HR; Hui SR; Calhoun BW; Manning DW; Kelly TJ; Lee S; Baron BW
    Vox Sang; 2008 Apr; 94(3):216-220. PubMed ID: 18167163
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Kell and XK immunohistochemistry in McLeod myopathy.
    Jung HH; Russo D; Redman C; Brandner S
    Muscle Nerve; 2001 Oct; 24(10):1346-51. PubMed ID: 11562915
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Acanthocytosis in chronic septic granulomatosis: the McLeod syndrome].
    Höger P; Seger R; Schenker T; Daniels GL; Irle U
    Monatsschr Kinderheilkd; 1985 May; 133(5):296-9. PubMed ID: 4040211
    [TBL] [Abstract][Full Text] [Related]  

  • 18. McLeod syndrome: a neurohaematological disorder.
    Jung HH; Danek A; Frey BM
    Vox Sang; 2007 Aug; 93(2):112-21. PubMed ID: 17683354
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A family of McLeod syndrome, masquerading as chorea-acanthocytosis.
    Takashima H; Sakai T; Iwashita H; Matsuda Y; Tanaka K; Oda K; Okubo Y; Reid ME
    J Neurol Sci; 1994 Jun; 124(1):56-60. PubMed ID: 7931422
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Haematological changes associated with the McLeod phenotype of the Kell blood group system.
    Wimer BM; Marsh WL; Taswell HF; Galey WR
    Br J Haematol; 1977 Jun; 36(2):219-24. PubMed ID: 871435
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.