biomedicina slovenica

re="Acta Myol" : 10

1. Meznarič Marija; Gradišnik Peter; Garavaglia Barbara; Lamantea Elenora; Lamperti Costanza; Zeviani Massimo
   A novel mitochondrial DNA mutation in the tRNASer(AGY) gene un a 12-year old boy with exercise intolerance
   2010 ►
2. Zidar J
   Clinical electrophysiological investigations in neuromuscular disorders
   2004 ►
3. Zupan A
   Device for stretching contractures in muscular dystrophy patients
   2002 ►
4. Canki-Klain N; Milic A; Kovac B; Trlaja A; Grgicevic D; Zurak N; Feingold J
   Carrier frequency of 550delA mutation of CAPN3 gene in Croatia
   2002 ►
5. Tupković E; Sinanović O; Zidar J
   Influence of depth of insertion of the electromyographic concentric needle electrode on the motor unit potentials in myopathic muscle
   2002 ►
6. Kalaydjieva L; King R; Gresham D; Molnar M; Tournev I; Angelicheva D; Butinar D; Colomer J; Corches A; Lupu C
   Hereditary motor and sensory neuropathy Lom
   2001 ►
7. Meznarič-Petruša M; Neubauer D; Teran N; Dolenšek J; Paro D; Peterlin B; Zidar J
   Neonatal muscle biopsy findings as the first clue of congenital myotonic dystrophy
   2002 ►
8. Butinar D; Starr A
   Auditory neuropathy in HMSN- Lom
   2001 ►
9. Meznarič-Petruša Mija; Zidar Janez
   Sarcoglycanopathy in two generations of the same family
   2000 ►
10. Leonardis Lea; Zidar Janez; Rautenstrauss Bernd
    Specific genotypes can only partly explain the great variability in the Charcot-Marie-tooth 1A disease phenotype
    2000 ►

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