Ralf Krahe und Myotonic - Info zur Person

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Cortical and Subcortical Grey and White Matter Atrophy in Myotonic...

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Other conributors: Ralf Krahe (Editor). License: This is an open access article distributed under the terms of the Creative Commons Attribution ...

Myotonic dystrophy phenotype without expansion of (CTG)n repeat: An...

link.springer.com

... phenotype without expansion of (CTG)n repeat: An entity distinct from proximal myotonic myopathy (PROMM)?. Authors; Authors and affiliations. Claudia Abbruzzese; Ralf Krahe; Michele Liguori; Daniela Tessarolo; Michael J. Siciliano; Tetsuo AshizawaEmail author; Manlio Giacanelli. Claudia Abbruzzese. 1. Ralf Krahe.

"The unstable (CTG)(n) trinucleotide repeat associated with myotonic...

digitalcommons.library.tmc.edu

The unstable (CTG)$\sb{\rm n}$ trinucleotide repeat associated with myotonic dystrophy: What it does and where it came from. Ralf Krahe, The University of Texas Grad ...

Population frequency of myotonic dystrophy: Higher than expected...

moh-it.pure.elsevier.com

Tiina Suominen, Linda L. Bachinski, Satu Auvinen, Peter Hackman, Keith A. Baggerly, Corrado Angelini, Leena Peltonen, Ralf Krahe, Bjarne Udd.

Myotonic dystrophy type 2 found in two of sixty-three persons...

researchportal.helsinki.fi

Satu Auvinen, Tiina Suominen, Pekka Hannonen, Linda L Bachinski, Ralf Krahe, Bjarne Udd. Department of Medical and Clinical Genetics.

Myotonic dystrophy type 2: clinical and genetic aspects —...

researchportal.helsinki.fi

Myotonic dystrophy type 2: clinical and genetic aspects. Ralf Krahe, Linda L Bachinski, Bjarne Udd. Research output: Chapter in Book/Report/Conference ...

GSE Skeletal muscle biopsies of patients with myotonic dystrophy...

medworm.com

A summary of this report with MedWorm recommendations of related news links and other reading to help further your research.

The myotonic dystrophies: molecular, clinical, and the…utic...

pubmed.ncbi.nlm.nih.gov

Lancet Neurol Oct;11(10): doi: S (12) Authors. Bjarne Udd , Ralf Krahe. Affiliation. 1 Neuromuscular Research Unit, ...

Myotonic dystrophy phenotype without expansion of (CTG)n repeat: An...

scholars.houstonmethodist.org

Myotonic dystrophy phenotype without expansion of (CTG)n repeat: An entity distinct from proximal myotonic myopathy (PROMM)?. Research output: Contribution to journal › Article. Claudia Abbruzzese, Ralf Krahe, Michele Liguori, Daniela Tessarolo, Michael J. Siciliano, Tetsuo Ashizawa, Manlio Giacanelli. Research ...

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Ralf Krahe und Myotonic Person-Info

Cortical and Subcortical Grey and White Matter Atrophy in Myotonic...

Myotonic dystrophy phenotype without expansion of (CTG)n repeat: An...

"The unstable (CTG)(n) trinucleotide repeat associated with myotonic...

Population frequency of myotonic dystrophy: Higher than expected...

Myotonic dystrophy type 2 found in two of sixty-three persons...

Myotonic dystrophy type 2: clinical and genetic aspects —...

GSE Skeletal muscle biopsies of patients with myotonic dystrophy...

The myotonic dystrophies: molecular, clinical, and the…utic...

Myotonic dystrophy phenotype without expansion of (CTG)n repeat: An...

Most expression and splicing changes in myotonic dystrophy type 1 and...

UT GSBS Dissertations (via ProQuest) from | Graduate...

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