M. Danon

发表

Exercise‐induced cramp, myoglobinuria, and tubular aggregates in phosphoglycerate mutase deficiency

S. Dimauro, K. Park, Shin J Oh, 2006, Muscle & nerve.

Muscle pain associated with tubular aggregates and structures resembling cylindrical spirals

S. Carpenter, Y. Harati, M. Danon, 1989, Muscle & nerve.

Quadriplegic areflexic ICU illness: Selective thick filament loss and normal nerve histology

H. Sander, M. Danon, M. Golden, 2002, Muscle & nerve.

Myopathy with thick filament (myosin) loss following prolonged paralysis with vecuronium during steroid treatment

S. Carpenter, M. Danon, 1991, Muscle & nerve.

Anti-neutrophil Cytoplasmic Antibody (c-ANCA) Positive Recurrent Eosinophilic Fasciitis Responsive to Cyclophosphamide

K. Kirou, M. Danon, D. Erkan, 2008, HSS Journal.

Guidelines for the diagnosis and treatment of chronic inflammatory demyelinating polyneuropathy

R. Freeman, W. Engel, M. Dalakas, 2003, Journal of the peripheral nervous system : JPNS.

Lysophosphatidylcholine-induced lysis of erythrocytes in Duchenne and myotonic dystrophies and in Huntington's disease

G. Sarpel, A. Barr, A. Omachi, 1982, Journal of the Neurological Sciences.

Human muscle proteins

N. Anderson, C. Giometti, M. Danon, 1983, Neurology.

Enzyme replacement therapy in the mouse model of Pompe disease.

N. Raben, R. Mattaliano, K. Nagaraju, 2003, Molecular genetics and metabolism.

Heterotopic neogenesis of skeletal muscle induced in the adult rat diaphragmatic peritoneum: ultrastructural and transplantation studies.

M. Danon, A. B. Drakontides, S. Levine, 1999, Histology and histopathology.

Tubular aggregates: their association with myalgia.

Y. Harati, M. Danon, E. Niakan, 1985, Journal of neurology, neurosurgery, and psychiatry.

Inverse relationship of skeletal muscle glycogen from wild-type and genetically modified mice to their phosphorylase a activity.

M. Danon, L. Schliselfeld, 2002, Biochemical and biophysical research communications.

Muscle glycogen of steroid myopathy patients

M. Danon, L. Schliselfeld, 1996, Journal of the Neurological Sciences.

Use of fructose-2,6-diphosphate to assay for phosphofructokinase activity in human muscle.

M. Danon, L. Schliselfeld, 1996, Clinical biochemistry.

Juvenile‐onset acid maltase deficiency with unusual familial features

S. Dimauro, M. Danon, A. Miranda, 1986, Neurology.

IL-10 production in common variable immunodeficiency.

C. Cunningham-Rundles, R. Huang, M. Danon, 1998, Clinical immunology and immunopathology.

Adult-onset nemaline rods in a patient treated for suspected dermatomyositis. Study with two-dimensional electrophoresis.

J. Skosey, C. Giometti, M. Danon, 1981, Archives of neurology.

Surprises of genetic engineering

S. Dimauro, P. Roach, N. Raben, 2001, Neurology.

Fatal infantile glycogen storage disease

S. Carpenter, M. Danon, J. Manaligod, 1981, Neurology.

Characterization of the enzymatic defect in late-onset muscle phosphofructokinase deficiency. New subtype of glycogen storage disease type VII.

S. Dimauro, D. Harker, M. Danon, 1987, The Journal of clinical investigation.

Hereditary sensory neuropathy

S. Carpenter, M. Danon, 1985, Neurology.

Nonprogressive congenital neuromuscular disease with uniform type 1 fiber.

S. Oh, M. Danon, 1983, Archives of neurology.

Erythrocyte membrane lysophospholipase activity in muscular dystrophy

G. Sarpel, A. Omachi, J. Podolski, 1983, Journal of the Neurological Sciences.

ERYTHROCYTE MEMBRANE LYSOPHOSPHOLIPASE IN MUSCULAR DYSTROPHY

J. Podolski, M. Danon, H. Lubansky, 1983 .

Early features of zidovudine-associated myopathy: histopathological findings and clinical correlations

M. Dalakas, M. Ropka, C. Jay, 2004, Acta Neuropathologica.

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

S. Dimauro, E. Schon, H. Tritschler, 1992, Neurology.

Clenbuterol reduces degeneration of exercised or aged dystrophic (mdx) muscle

M. Danon, J. D. Etlinger, R. Zeman, 2000, Muscle & nerve.

Late‐onset muscle phosphofructokinase deficiency

S. Dimauro, S. Servidei, M. Danon, 1988, Neurology.

Peripheral polyneuropathy associated with primary malignant lymphoma of the brain.

J. Chusid, M. Danon, H. Donnenfeld, 1978, Archives of neurology.

Inclusion body myositis. A corticosteroid-resistant idiopathic inflammatory myopathy.

J. Masdeu, M. Reyes, M. Danon, 1982, Archives of neurology.

Lysosomal glycogen storage disease with normal acid maltase

S. Dimauro, S. Naidu, M. Danon, 1981, Neurology.

Gene expression profiling in chronic inflammatory demyelinating polyneuropathy

M. Dalakas, A. Hays, N. Latov, 2005, Journal of Neuroimmunology.

Inclusion Body Myositis Associated with Systemic Sarcoidosis

M. Danon, S. Ronan, J. Manaligod, 1986, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Erythrocytes in muscular dystrophy. Investigation with 31P nuclear magnetic resonance spectroscopy.

G. Sarpel, A. Omachi, M. Danon, 1981, Archives of neurology.

Erythrocyte metabolism in muscular dystrophy.

G. Sarpel, A. Omachi, W. Marshall, 1978, Archives of neurology.

Sarcoplasmic reticulum adenosine triphosphatase deficiency with probable autosomal dominant inheritance

M. Danon, G. Karpati, J. Charuk, 1988, Neurology.

Hypokalemic periodic paralysis with unusual responses to acetazolamide and sympathomimetics

M. Danon, B. Vern, K. Hanlon, 1987, Journal of the Neurological Sciences.

Study of skeletal muscle glycogenolysis and glycolysis in chronic steroid myopathy, non-steroid histochemical type-2 fiber atrophy, and denervation.

M. Danon, L. Schliselfeld, 2006, Clinical biochemistry.

Heterogeneity of human skeletal muscle tropomyosin

C. Giometti, M. Danon, Moris J. Danon, 1985, Annals of neurology.

Inclusion body myositis. A corticosteroid-resistant idiopathic inflammatory myopathy.

J. Masdeu, M. Reyes, M. Danon, 1982, Archives of neurology.

Inclusion Body Myositis Associated with Progressive Dysphagia: Treatment with Cricopharyngeal Myotomy

M. Friedman, M. Danon, 1989, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.