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hormone deficiency
Person
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Person
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doc. MUDr. Miluše Havlová CSc.
Person without affiliation with CUNI
50 publications
Publications
publication
Mosaicism for GJB1 mutation causes milder Charcot-Marie-Tooth X1 phenotype in a heterozygous man than in a manifesting heterozygous woman
2013 |
Second Faculty of Medicine, Faculty of Science, First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Adult Form of Glutaric Aciduria Type II - Underdiagnosed Cause of Proximal Myopathy - a Case Report
2009 |
Second Faculty of Medicine
publication
Post-poliomyelitic syndrome
2006 |
First Faculty of Medicine
publication
Spinal muscular atrophy
2006 |
First Faculty of Medicine
publication
Alternating hemiplegia of childhood (AHC)
2005 |
First Faculty of Medicine
publication
Postpoliomyelitic syndrome
2005 |
Publication without faculty affiliation
publication
Molecular-pathologic and genetic diagnostics of limb girdle muscular dystrophy LGMD2A: presentation of first cases diagnosed in the Czech republik
2004 |
First Faculty of Medicine
publication
The Centre for neuromuscular disorders in Neurological department of General hospital
2003 |
First Faculty of Medicine
publication
Cardiological findings in patients with progressive muscular dystrophy
2003 |
First Faculty of Medicine
publication
Problems of Postpoliomyelitic syndrome
2002 |
First Faculty of Medicine
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