Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 36

1.

Acanthocytes in the McLeod phenotype of X-linked chronic granulomatous disease.

Beaulieu GP, Ward DC, Panch SR, Flegel WA.

Transfusion. 2017 Oct;57(10):2307-2308. doi: 10.1111/trf.14119. No abstract available.

PMID:
28944547
2.

Stepwise partitioning of Xp21: a profiling method for XK deletions causative of the McLeod syndrome.

Gassner C, Brönnimann C, Merki Y, Mattle-Greminger MP, Sigurdardottir S, Meyer E, Engström C, O'Sullivan JD, Jung HH, Frey BM.

Transfusion. 2017 Sep;57(9):2125-2135. doi: 10.1111/trf.14172. Epub 2017 May 28.

PMID:
28555782
3.

Clinical variability of neuroacanthocytosis syndromes-a series of six patients with long follow-up.

Dulski J, Sołtan W, Schinwelski M, Rudzińska M, Wójcik-Pędziwiatr M, Wictor L, Schön F, Puschmann A, Klempíř J, Tilley L, Roth J, Tacik P, Fujioka S, Drozdowski W, Sitek EJ, Wszolek Z, Sławek J.

Clin Neurol Neurosurg. 2016 Aug;147:78-83. doi: 10.1016/j.clineuro.2016.05.028. Epub 2016 Jun 1.

PMID:
27310290
4.

Kell and Kx blood group systems.

Denomme GA.

Immunohematology. 2015;31(1):14-9. Review.

PMID:
26308465
5.

Neurodegeneration in the elderly - When the blood type matters: An overview of the McLeod syndrome with focus on hematological features.

Frey BM, Gassner C, Jung HH.

Transfus Apher Sci. 2015 Jun;52(3):277-84. doi: 10.1016/j.transci.2015.04.007. Epub 2015 Apr 14. Review.

6.

Acanthocytosis and the c.680 A>G Mutation in the PANK2 Gene: A Study Enrolling a Cohort of PKAN Patients from the Dominican Republic.

Schiessl-Weyer J, Roa P, Laccone F, Kluge B, Tichy A, De Almeida Ribeiro E, Prohaska R, Stoeter P, Siegl C, Salzer U.

PLoS One. 2015 Apr 27;10(4):e0125861. doi: 10.1371/journal.pone.0125861. eCollection 2015.

7.

O'Sullivan-McLeod syndrome: clinical features, neuroradiology and nosology.

Ghadiri-Sani M, Huda S, Larner AJ.

Br J Hosp Med (Lond). 2014 Dec;75(12):712-3. doi: 10.12968/hmed.2014.75.12.712. No abstract available.

PMID:
25488537
8.

The first report of a Chinese family with McLeod syndrome.

Man BL, Yuen YP, Fu YP.

BMJ Case Rep. 2014 Jun 3;2014. pii: bcr2013202785. doi: 10.1136/bcr-2013-202785.

9.

Differential diagnosis of Huntington's disease: what the clinician should know.

Cardoso F.

Neurodegener Dis Manag. 2014;4(1):67-72. doi: 10.2217/nmt.13.78.

PMID:
24640980
10.

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 15;340(1-2):221-4. doi: 10.1016/j.jns.2014.02.027. Epub 2014 Feb 27.

PMID:
24635891
11.

Abnormal red cell features associated with hereditary neurodegenerative disorders: the neuroacanthocytosis syndromes.

De Franceschi L, Bosman GJ, Mohandas N.

Curr Opin Hematol. 2014 May;21(3):201-9. doi: 10.1097/MOH.0000000000000035. Review.

PMID:
24626044
12.

Novel single base-pair deletion in exon 1 of XK gene leading to McLeod syndrome with chorea, muscle wasting, peripheral neuropathy, acanthocytosis and haemolysis.

Wiethoff S, Xiromerisiou G, Bettencourt C, Kioumi A, Tsiptsios I, Tychalas A, Evaggelia M, George K, Makris V, Hardy J, Houlden H.

J Neurol Sci. 2014 Apr 15;339(1-2):220-2. doi: 10.1016/j.jns.2014.01.034. Epub 2014 Feb 1.

13.

VATS bullectomy and apical pleurectomy for spontaneous pneumothorax in a young patient with Swyer-James-Mc Leod syndrome: case report presentation and literature review focusing on surgically treated cases.

Panagopoulos N, Papavasileiou G, Koletsis E, Kastanaki M, Anastasiou N.

J Cardiothorac Surg. 2014 Jan 10;9:13. doi: 10.1186/1749-8090-9-13. Review.

14.

Giant axon formation in mice lacking Kell, XK, or Kell and XK: animal models of McLeod neuroacanthocytosis syndrome.

Zhu X, Cho ES, Sha Q, Peng J, Oksov Y, Kam SY, Ho M, Walker RH, Lee S.

Am J Pathol. 2014 Mar;184(3):800-7. doi: 10.1016/j.ajpath.2013.11.013. Epub 2014 Jan 7.

15.

Henry VIII, McLeod syndrome and Jacquetta's curse.

Stride P, Lopes Floro K.

J R Coll Physicians Edinb. 2013;43(4):353-60. doi: 10.4997/JRCPE.2013.417.

PMID:
24350322
16.

Alterations of red cell membrane properties in neuroacanthocytosis.

Siegl C, Hamminger P, Jank H, Ahting U, Bader B, Danek A, Gregory A, Hartig M, Hayflick S, Hermann A, Prokisch H, Sammler EM, Yapici Z, Prohaska R, Salzer U.

PLoS One. 2013 Oct 3;8(10):e76715. doi: 10.1371/journal.pone.0076715. eCollection 2013.

17.

The first case report of McLeod syndrome in a Chinese patient.

Man BL, Yuen YP, Yip SF, Ng SH.

BMJ Case Rep. 2013 Aug 13;2013. pii: bcr2013200205. doi: 10.1136/bcr-2013-200205. Review.

18.

A case of McLeod phenotype of neuroacanthocytosis brain MR features and literature review.

Shah JR, Patkar DP, Kamat RN.

Neuroradiol J. 2013 Feb;26(1):21-6. Epub 2013 Mar 8. Review.

19.

The chorea of McLeod syndrome: progression to hypokinesia.

Miranda M, Jung HH, Danek A, Walker RH.

Mov Disord. 2012 Nov;27(13):1701-2. doi: 10.1002/mds.25224. No abstract available.

PMID:
23192927
20.

Computational identification of phospho-tyrosine sub-networks related to acanthocyte generation in neuroacanthocytosis.

De Franceschi L, Scardoni G, Tomelleri C, Danek A, Walker RH, Jung HH, Bader B, Mazzucco S, Dotti MT, Siciliano A, Pantaleo A, Laudanna C.

PLoS One. 2012;7(2):e31015. doi: 10.1371/journal.pone.0031015. Epub 2012 Feb 15.

Supplemental Content

Loading ...
Support Center