Günter Scheuerbrandt: search on Z-Library

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1

Screening for duchenne muscular dystrophy: An improved screening test for creatine kinase and its application in an infant screening program

Dr. Günter Scheuerbrandt, Mr. Arne Lundin, Dr. Timo Lövgren, Dr. Wilhelm Mortier

Journal:

Year:

1986

Language:

english

File:

PDF, 1.08 MB

english, 1986

2

Screening for Duchenne muscular dystrophy in Germany, 1977-2011: A personal story

Scheuerbrandt, Günter

Journal:

Year:

2017

Language:

english

File:

PDF, 714 KB

english, 2017

3

Additional techniques for submicro CHN-analysis: Extension of sample range, combustion of liquids and hygroscopic compounds

Walter Walisch, Günter Scheuerbrandt, Werner Marks

Journal:

Microchemical Journal

Year:

1966

Language:

english

File:

PDF, 390 KB

english, 1966

4

Automatic determination of the decarboxylase for aromatic amino acids in mouse liver

Günter Scheuerbrandt

Journal:

Analytical Biochemistry

Year:

1965

Language:

english

File:

PDF, 430 KB

english, 1965

5

High levels of brain-type creatine kinase activity in human platelets and leukocytes: A genetic anomaly with autosomal dominant inheritance

Heidwolf Arnold, Thomas F. Wienker, Michael M. Hoffmann, Günter Scheuerbrandt, Katharina Kemp, Peter Bugert

Journal:

Blood Cells, Molecules, and Diseases

Year:

2012

Language:

english

File:

PDF, 627 KB

english, 2012

6

EARLY DIAGNOSIS OF DUCHENNE MUSCULAR DYSTROPHY

Beckmann, Robert, Sauer, Manfred, Ketelsen, Uwe-Peter, Scheuerbrandt, Gunter

Journal:

Year:

1978

Language:

english

File:

PDF, 162 KB

english, 1978

7

Identifying Non–Duchenne Muscular Dystrophy–Positive and False Negative Results in Prior Duchenne Muscular Dystrophy Newborn Screening Programs

Gatheridge, Michele A., Kwon, Jennifer M., Mendell, Jerry M., Scheuerbrandt, Günter, Moat, Stuart J., Eyskens, François, Rockman-Greenberg, Cheryl, Drousiotou, Anthi, Griggs, Robert C.

Journal:

Year:

2015

Language:

english

File:

PDF, 113 KB

english, 2015

8

Creatine kinase in human erythrocytes: A genetic anomaly reveals presence of soluble brain-type isoform

Kay, Laurence, Tokarska-Schlattner, Malgorzata, Quenot-Carrias, Bénédicte, Goudet, Betty, Bugert, Peter, Arnold, Heidwolf, Scheuerbrandt, Günter, Schlattner, Uwe

Journal:

Blood Cells, Molecules, and Diseases

Year:

2017

Language:

english

File:

PDF, 731 KB

english, 2017