Frey BM - Search Results

1

McLeod syndrome: a neurohaematological disorder.

Jung HH, Danek A, Frey BM. Jung HH, et al. Among authors: frey bm. Vox Sang. 2007 Aug;93(2):112-21. doi: 10.1111/j.1423-0410.2007.00949.x. Vox Sang. 2007. PMID: 17683354 Review.

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. Jung HH, et al. Among authors: frey bm. Transfusion. 2003 Jul;43(7):928-38. doi: 10.1046/j.1537-2995.2003.t01-1-00434.x. Transfusion. 2003. PMID: 12823753

3

Phenotypic variability of a distinct deletion in McLeod syndrome.

Miranda M, Castiglioni C, Frey BM, Hergersberg M, Danek A, Jung HH. Miranda M, et al. Among authors: frey bm. Mov Disord. 2007 Jul 15;22(9):1358-61. doi: 10.1002/mds.21536. Mov Disord. 2007. PMID: 17469188

4

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. Frey BM, et al. Transfus Apher Sci. 2015 Jun;52(3):277-84. doi: 10.1016/j.transci.2015.04.007. Epub 2015 Apr 14. Transfus Apher Sci. 2015. PMID: 25934153 Free article. Review.

5

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. Gassner C, et al. Among authors: frey bm. Transfusion. 2017 Sep;57(9):2125-2135. doi: 10.1111/trf.14172. Epub 2017 May 28. Transfusion. 2017. PMID: 28555782

6

Molecular Basis and Clinical Overview of McLeod Syndrome Compared With Other Neuroacanthocytosis Syndromes: A Review.

Roulis E, Hyland C, Flower R, Gassner C, Jung HH, Frey BM. Roulis E, et al. Among authors: frey bm. JAMA Neurol. 2018 Dec 1;75(12):1554-1562. doi: 10.1001/jamaneurol.2018.2166. JAMA Neurol. 2018. PMID: 30128557 Free article. Review.

7

WITHDRAWN: Novel Xp21.1 deletion associated with unusual features in a large McLeod syndrome kindred.

Sveinsson O, Udd B, Svenningsson P, Gassner C, Engström C, Laffita-Mesa JM, Solders G, Hertegård S, Savitcheva I, Jung HH, Tolnay M, Frey BM, Paucar M. Sveinsson O, et al. Among authors: frey bm. Parkinsonism Relat Disord. 2018 Oct 8:S1353-8020(18)30399-7. doi: 10.1016/j.parkreldis.2018.09.014. Online ahead of print. Parkinsonism Relat Disord. 2018. PMID: 30305234 No abstract available.

8

Involuntary movements, vocalizations and cognitive decline.

Sveinsson O, Udd B, Svenningsson P, Gassner C, Engström C, Laffita-Mesa J, Solders G, Hertegård S, Savitcheva I, Jung HH, Tolnay M, Frey BM, Paucar M. Sveinsson O, et al. Among authors: frey bm. Parkinsonism Relat Disord. 2020 Oct;79:135-137. doi: 10.1016/j.parkreldis.2019.05.029. Epub 2019 May 29. Parkinsonism Relat Disord. 2020. PMID: 31153763 No abstract available.

9

A uniform method for the simultaneous blood group phenotyping of Fy^a , Fy^b , Jk^a , Jk^b , S, s̅, P1, k applying lateral-flow technique.

Caesar A, Meyer S, Trost N, Neuenschwander K, Geisen C, Frey BM, Gassner C, Schwind P. Caesar A, et al. Among authors: frey bm. Vox Sang. 2018 Feb;113(2):177-184. doi: 10.1111/vox.12603. Epub 2017 Oct 16. Vox Sang. 2018. PMID: 29044588

10

Novel regulatory variant in ABO intronic RUNX1 binding site inducing A₃ phenotype.

Thun GA, Gueuning M, Sigurdardottir S, Meyer E, Gourri E, Schneider L, Merki Y, Trost N, Neuenschwander K, Engström C, Frey BM, Meyer S, Mattle-Greminger MP. Thun GA, et al. Among authors: frey bm. Vox Sang. 2024 Apr;119(4):377-382. doi: 10.1111/vox.13580. Epub 2024 Jan 16. Vox Sang. 2024. PMID: 38226545

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