Results 141 to 150 of about 988,052 (165)
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Neonatal metabolic myopathies

Seminars in Perinatology, 1999
The primary presentations of neuromuscular disease in the newborn period are hypotonia and weakness. Although metabolic myopathies are inherited disorders that present from birth and may present with subtle to marked neonatal hypotonia, a number of these defects are diagnosed classically in childhood, adolescence, or adulthood.
openaire   +2 more sources

Metabolic and mitochondrial myopathies

Current Opinion in Rheumatology, 1989
Metabolic myopathies are the result of genetic defects that cause disordered energy metabolism. These diseases can cause a variety of myopathic syndromes and can become clinically manifest at any age. Recent advances in the understanding of the molecular and metabolic bases for these diseases have resulted in expanded clinical descriptions, recognition
openaire   +3 more sources

Metabolic Myopathies

Medical Clinics of North America, 1979
E P, Bosch, T L, Munsat
openaire   +2 more sources

METABOLIC MYOPATHIES

Acta Neurologica Scandinavica, 2009
Mark Oette   +194 more
openaire   +3 more sources

Metabolic myopathies

Neurologie pro praxi, 2022
Hana Kolářová, Pavel Ješina
openaire   +1 more source

Metabolic Oncologic Emergencies

Ca-A Cancer Journal for Clinicians, 1987
John H Glick
exaly  

A Diagnostic Algorithm for Metabolic Myopathies

Current Neurology and Neuroscience Reports, 2010
Michio Hirano   +2 more
exaly  

Metabolic Myopathies: Clinical Features and Diagnostic Approach

Rheumatic Disease Clinics of North America, 2011
Areeg El-Gharbawy   +2 more
exaly  

Congenital and Metabolic Myopathies of Childhood or Adult Onset

Seminars in Arthritis and Rheumatism, 2000
Josep Maria Grau   +2 more
exaly  

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