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Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene

Clinical genetics, 2012-07, Vol.82 (1), p.88-92

2012

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Phase II study of eribulin mesylate (E7389) in patients with metastatic castration-resistant prostate cancer stratified by prior taxane therapy

Annals of oncology, 2012-05, Vol.23 (5), p.1241-1249

2012

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Molecular and imaging correlates of the fragile X-associated tremor/ataxia syndrome

Neurology, 2006-10, Vol.67 (8), p.1426-1431

2006

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Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion

Clinical genetics, 2015-02, Vol.87 (2), p.173-178

2015

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Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism

Clinical genetics, 2009-11, Vol.76 (5), p.471-476

2009

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Gesundheit am Arbeitsplatz Kindertagesstätte

Arbeitsmedizin, Sozialmedizin, Umweltmedizin, 2018, Vol.53 (3), p.193-196

Losch, D

2018

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White matter changes in basis pontis in small expansion FMR1 allele carriers with parkinsonism

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011-06, Vol.156B (4), p.502-506

2011

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New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease

Clinical genetics, 2013-10, Vol.84 (4), p.382-385

2013

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Mobiltelefone im Krankenhaus

Zentralblatt für Arbeitsmedizin, Arbeitsschutz und Ergonomie, 2016-09, Vol.66 (5), p.316-317

Losch, D.

2016

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Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond

Clinical genetics, 2005-05, Vol.67 (5), p.412-417

2005

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Combination Versus Sequential Doxorubicin and Docetaxel as Primary Chemotherapy for Breast Cancer: A Randomized Pilot Trial of the Hoosier Oncology Group

Journal of clinical oncology, 1999-10, Vol.17 (10), p.3033-3037

1999

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Secular trend in body height and weight of Australian children and adolescents

American journal of physical anthropology, 2000-04, Vol.111 (4), p.545-556

2000

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A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes

Journal of medical genetics, 2008-03, Vol.45 (3), p.179-181

2008

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Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis

American journal of medical genetics, 2003-09, Vol.122A (1), p.13-23

2003

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Protein profiling of ovarian cancers by immunohistochemistry to identify potential target pathways

Gynecologic oncology, 2012-03, Vol.125, p.S91-S91

2012

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Phase 3 Trial of Everolimus for Metastatic Renal Cell Carcinoma: Final Results and Analysis of Prognostic Factors

Cancer, 2010-09, Vol.116 (18), p.4256-4265

2010

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Tremor/ataxia syndrome and fragile X premutation: Diagnostic caveats

Journal of clinical neuroscience, 2007-03, Vol.14 (3), p.245-248

2007

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Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: A new perspective

American journal of medical genetics, 2003-04, Vol.118A (2), p.127-134

2003

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Efficacy of everolimus in advanced renal cell carcinoma: a double-blind, randomised, placebo-controlled phase III trial

The Lancet (British edition), 2008-08, Vol.372 (9637), p.449-456

2008

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Schlafstörungen und Arbeitsunfähigkeit in Deutschland

Zentralblatt für Arbeitsmedizin, Arbeitsschutz und Ergonomie, 2017-11, Vol.67 (6), p.342-344

2017

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Abstract P3-11-17: A novel biodynamic imaging assay predicts success or failure of neoadjuvant chemotherapy in breast cancer patients

Cancer research (Chicago, Ill.), 2019-02, Vol.79 (4_Supplement), p.P3-P3-11-17

2019

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FMR1 alleles in Tasmania: a screening study of the special educational needs population

Clinical genetics, 2005-01, Vol.67 (1), p.38-46

2005

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Handynacken

Zentralblatt für Arbeitsmedizin, Arbeitsschutz und Ergonomie, 2017-07, Vol.67 (4), p.234-236

2017

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Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism

Genetics in medicine, 2011-05, Vol.13 (5), p.392-399

2011

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Genotype-phenotype relationships in fragile X syndrome : a family study

American journal of human genetics, 1993-11, Vol.53 (5), p.1064-1073

1993

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Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene

Phase II study of eribulin mesylate (E7389) in patients with metastatic castration-resistant prostate cancer stratified by prior taxane therapy

Molecular and imaging correlates of the fragile X-associated tremor/ataxia syndrome

Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion

Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism

Gesundheit am Arbeitsplatz Kindertagesstätte

White matter changes in basis pontis in small expansion FMR1 allele carriers with parkinsonism

New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease

Mobiltelefone im Krankenhaus

Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond

Combination Versus Sequential Doxorubicin and Docetaxel as Primary Chemotherapy for Breast Cancer: A Randomized Pilot Trial of the Hoosier Oncology Group

Secular trend in body height and weight of Australian children and adolescents

A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes

Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis

Protein profiling of ovarian cancers by immunohistochemistry to identify potential target pathways

Phase 3 Trial of Everolimus for Metastatic Renal Cell Carcinoma: Final Results and Analysis of Prognostic Factors

Tremor/ataxia syndrome and fragile X premutation: Diagnostic caveats

Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: A new perspective

Efficacy of everolimus in advanced renal cell carcinoma: a double-blind, randomised, placebo-controlled phase III trial

Schlafstörungen und Arbeitsunfähigkeit in Deutschland

Abstract P3-11-17: A novel biodynamic imaging assay predicts success or failure of neoadjuvant chemotherapy in breast cancer patients

FMR1 alleles in Tasmania: a screening study of the special educational needs population

Handynacken

Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism

Genotype-phenotype relationships in fragile X syndrome : a family study

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