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1

Diagnostik von Myopathien

Deschauer, M., Müller-Reible, C., Rösler, K., Schoser, B., Wanschitz, J., Weis, J., Zierz, S.

Journal:

Aktuelle Neurologie

Year:

2016

File:

PDF, 251 KB

2016

2

De-duplicating patient records from three independent data sources reveals the incidence of rare neuromuscular disorders in Germany

König, Kirsten, Pechmann, Astrid, Thiele, Simone, Walter, Maggie C., Schorling, David, Tassoni, Adrian, Lochmüller, Hanns, Müller-Reible, Clemens, Kirschner, Janbernd

Journal:

Orphanet Journal of Rare Diseases

Year:

2019

Language:

english

File:

PDF, 814 KB

english, 2019

3

Fazioskapulohumerale Muskeldystrophie

B. Jordan, C. Müller-Reible, S. Zierz

Journal:

Year:

2011

Language:

german

File:

PDF, 547 KB

german, 2011

4

Genetik und Klinik der Hämophilie A und B

R. Schwaab, S. Rost, J. Schröder, C.R. Müller-Reible, J. Oldenburg

Journal:

medizinische genetik

Year:

2008

Language:

german

File:

PDF, 361 KB

german, 2008

5

Pharmakogenetik der oralen Antikoagulation mit Cumarinen

J. Oldenburg, S. Rost, H. Seidel, M. Watzka, C.R. Müller-Reible

Journal:

medizinische genetik

Year:

2008

Language:

german

File:

PDF, 346 KB

german, 2008

6

Qualitätssicherung wird europäisch!

C.R. Müller-Reible

Journal:

medizinische genetik

Year:

2008

Language:

german

File:

PDF, 103 KB

german, 2008

7

Muskeldystrophien Duchenne und Becker

T. Grimm, W. Kress, G. Meng, C.R. Müller-Reible

Journal:

medizinische genetik

Year:

2009

Language:

german

File:

PDF, 392 KB

german, 2009

8

Heterozygous large deletions of Factor 8 gene in females identified by multiplex PCR-LC

A. PAVLOVA, T. FÖRSTER, D. DELEV, J. SCHRÖDER, O. EL-MAARRI, C. MÜLLER-REIBLE, J. OLDENBURG

Journal:

Year:

2008

Language:

english

File:

PDF, 408 KB

english, 2008

9

Novel RYR1 missense mutation causes core rod myopathy

M. Von Der Hagen, W. Kress, G. Hahn, K. S. Brocke, P. Mitzscherling, A. Huebner, C. Müller-Reible, G. Stoltenburg-Didinger, A. M. Kaindl

Journal:

European Journal of Neurology

Year:

2008

Language:

english

File:

PDF, 128 KB

english, 2008

10

Facing the genetic heterogeneity in neuromuscular disorders: Linkage analysis as an economic diagnostic approach towards the molecular diagnosis

M. von der Hagen, J. Schallner, A.M. Kaindl, K. Koehler, P. Mitzscherling, A. Abicht, U. Grieben, R. Korinthenberg, W. Kress, A. von Moers, J.S. Müller, U. Schara, M. Vorgerd, M.C. Walter, C. Müller-R

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 126 KB

english, 2006

11

P.P.6 03 Incidence of 550delA in the CAPN3 gene in German patients with limb-girdle muscular dystrophy and hyperCKemia

F. Hanisch, D. Grimm, L. Xue, C. Müller-Reible, S. Zierz, M. Deschauer

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 58 KB

english, 2006

12

G.P.4.14 Clinical variability in siblings with calpainopathy (LGMD2A)

J. Kirschner, J. Schessl, M. Walter, G. Schreiber, C. Müller-Reible, U. Schara, C. Bönnemann, R. Korinthenberg

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 48 KB

english, 2007

13

Regional lactate and carbon dioxide concentrations in a metabolic test for malignant hyperthermia

Martin Anetseder, Martin Hager, Clemens Müller-Reible, Norbert Roewer

Journal:

Year:

2003

Language:

english

File:

PDF, 45 KB

english, 2003

14

Environmental and genetic factors influencing inhibitor development

Johannes Oldenburg, Jörg Schröder, Hans Hermann Brackmann, Clemens Müller-Reible, Rainer Schwaab, Edward Tuddenham

Journal:

Seminars in Hematology

Year:

2004

Language:

english

File:

PDF, 116 KB

english, 2004

15

Applications and data analysis of next-generation sequencing

Vogl, Ina, Benet-Pagès, Anna, Eck, Sebastian H., Kuhn, Marius, Vosberg, Sebastian, Greif, Philipp A., Metzeler, Klaus H., Biskup, Saskia, Müller-Reible, Clemens, Klein, Hanns-Georg

Journal:

Laboratoriums Medizin

Year:

2013

File:

PDF, 2.54 MB

2013

16

[American Thoracic Society American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California - ()] A17. PATHOGENIC MECHANISMS OF ACUTE LUNG INJURY - Sphingosine Kinase-1 And Sphingosine-1-Phosphate Promote The Development Of Acute Lung Injury In Pneumoccocal Pneumonia

Gutbier, Birgitt, Schoenrock, Stefanie M., Haberberger, Rainer, Hocke, Andreas C., Hippenstiel, Stefan, Luth, Anja, Kleuser, Burkhard, Bertrams, Wilhelm G., Szymanski, Kolja, Reppe, Katrin, Muller-Red

Year:

2012

Language:

english

File:

PDF, 21 KB

english, 2012

17

Molekulargenetische Diagnostik der Myopathien

C. Müller-reible, W. Kress, G. Meng

Year:

2009

Language:

german

File:

PDF, 454 KB

german, 2009

18

SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorder

Merker, Sören, Reif, Andreas, Ziegler, Georg C., Weber, Heike, Mayer, Ute, Ehlis, Ann-Christine, Conzelmann, Annette, Johansson, Stefan, Müller-Reible, Clemens, Nanda, Indrajit, Haaf, Thomas, Ullmann,

Journal:

Journal of Child Psychology and Psychiatry

Year:

2017

Language:

english

File:

PDF, 528 KB

english, 2017

19

The Genetic Approach: Next-Generation Sequencing-Based Diagnosis of Congenital and Infantile Myopathies/Muscle Dystrophies

Kress, Wolfram, Rost, Simone, Kolokotronis, Konstantin, Meng, Gerhard, Pluta, Natalie, Müller-Reible, Clemens

Journal:

Neuropediatrics

Year:

2017

Language:

english

File:

PDF, 103 KB

english, 2017

20

Current pharmacogenetic developments in oral anticoagulation therapy: The influence of variant VKORC1 and CYP2C9 alleles

Oldenburg, Johannes, Bevans, Carville, Fregin, Andreas, Geisen, Christof, Müller-Reible, Clemens, Watzka, Matthias

Journal:

Thrombosis and Haemostasis

Year:

2007

Language:

english

File:

PDF, 756 KB

english, 2007

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