8 results on '"Piraud M"'
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2. Maladies héréditaires du métabolisme : signes anténatals et diagnostic biologique
3. Current French Pompe Prevalence Study (French PoPS)
4. Paraneoplastic dermatomyositis with glycogen accumulation in muscle
5. P.17.17 McArdle disease with pronounced axial myopathy
6. P5.48 Infantile-onset permanent weakness in muscle phosphofructokinase deficiency
7. G.P.16.09. Phosphoglucomutase deficiency: A rare glycogen storage disease with an adult onset
8. Diagnosis of mucopolysaccharidoses in a clinically selected population by urinary glycosaminoglycan analysis: A study of 2,000 urine samples
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