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Klinik und Poliklinik für Kinder- und Jugendmedizin

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Cobos, PN; Keil, A; Santer, R et al.

SELECTIVE SCREENING FOR POMPE DISEASE IN PATIENTS AFFECTED WITH PERSISTENT CK-ELEVATIONS OR LIMB MUSCLE DYSTROPHY

MOLECULAR GENETICS AND METABOLISM. Bd. 98. H. 1-2. 2009 S. 76-76



Nusslein, HG; Huppertz, HI; Massenkeil, G et al.

Splenomegaly - An Important Cardinal Symptom

AKTUELLE RHEUMATOLOGIE. Bd. 34. H. 4. 2009 S. 213-219


Rohrig, B; du Prel, JB; Blettner, M

Study Design in Medical Research Part 2 of a Series on the Evaluation of Scientific Publications

DEUTSCHES ARZTEBLATT INTERNATIONAL. Bd. 106. H. 11. 2009 S. 184-189


Pitz, S; Grube-Einwald, K; Renieri, G et al.

Subclinical optic neuropathy in Fabry disease.

Ophthalmic Genet. Bd. 30. H. 4. 2009 S. 165-71



Hendriksz, CJ; Valayannopoulos, V; Teles, EL et al.

THE FIRST REPORT OF THE MPS VI CLINICAL SURVEILLANCE PROGRAM (CSP)

MOLECULAR GENETICS AND METABOLISM. Bd. 98. H. 1-2. 2009 S. 1-1


Schneider, E; Lausch, E; Roos, F et al.

The protein phosphatase and the PDZ binding domain of the tumor suppressor PTEN regulate migration of renal cancer cells

EUROPEAN JOURNAL OF CELL BIOLOGY. Bd. 88. 2009 S. 80-80


Kampmann, C

The Thirty Years' War and German Memory in the Nineteenth Century

HISTORISCHE ZEITSCHRIFT. Bd. 288. H. 3. 2009 S. 690-691


Ozbek, MN; Uslu, AB; Onenli-Mungan, N et al.

Thyroid peroxidase gene mutations causing congenital hypothyroidism in three Turkish families

J Pediatr Endocrinol Metab. Bd. 22. H. 11. 2009 S. 1033-9