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Neurology
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March 1, 1994
Unusual expression and very mild course of Xp21 muscular dystrophy (Becker type) in a 60-year-old man with 26 percent deletion of the dystrophin gene
L Palmucci, C Doriguzzi, T Mongini, et al.
European Journal of Clinical Investigation
|
April 1, 1997
Systematic use of dystrophin testing in muscle biopsies: results in 201 cases
C Doriguzzi, L Palmucci, T Mongini, et al.
Neuropediatrics
|
June 21, 2002
Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria
T Mongini, C Doriguzzi, I Bosone, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 1, 1989
Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency
C Doriguzzi, L Palmucci, T Mongini, et al.
Neuropediatrics
|
June 21, 2001
Myopathy in a patient with chromosome 22q11 deletion
T Mongini, C Doriguzzi, C Arduino, et al.
Journal of the Neurological Sciences
|
February 1, 1986
Quantitative analysis of quadriceps muscle biopsy. Results in 7 definite and 45 possible carriers of Duchenne muscular dystrophy
C Doriguzzi, L Palmucci, T Mongini, et al.
Minerva Medica
|
September 15, 1980
[Progressive muscular dystrophy of the Duchenne type. Epidemiology and strategy for prevention]
C Doriguzzi, A Bertolotto, T Mongini, et al.
Italian Journal of Orthopaedics and Traumatology
|
December 1, 1984
Histomorphometric study of the dynamics of mineralization in a case of osteomalacia caused by anticonvulsants treated with 25(OH)d3
M Portigliatti Barbos, P Rossi, A Jeantet, et al.
European Journal of Histochemistry : EJH
|
January 1, 1994
Metachromatic dye-Ca++ATPase method in pathological muscle: a study of 382 muscle biopsies
C Doriguzzi, L Palmucci, T Mongini, et al.
Acta Neuropathologica
|
January 1, 1990
Cytochrome c oxidase and coenzyme Q in neuromuscular diseases: a histochemical study
C Doriguzzi, L Palmucci, B Pollo, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 55) with videos related to
Sort By:
Page
of 6
Neurology
|
March 1, 1994
Unusual expression and very mild course of Xp21 muscular dystrophy (Becker type) in a 60-year-old man with 26 percent deletion of the dystrophin gene
L Palmucci, C Doriguzzi, T Mongini, et al.
European Journal of Clinical Investigation
|
April 1, 1997
Systematic use of dystrophin testing in muscle biopsies: results in 201 cases
C Doriguzzi, L Palmucci, T Mongini, et al.
Neuropediatrics
|
June 21, 2002
Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria
T Mongini, C Doriguzzi, I Bosone, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 1, 1989
Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency
C Doriguzzi, L Palmucci, T Mongini, et al.
Neuropediatrics
|
June 21, 2001
Myopathy in a patient with chromosome 22q11 deletion
T Mongini, C Doriguzzi, C Arduino, et al.
Journal of the Neurological Sciences
|
February 1, 1986
Quantitative analysis of quadriceps muscle biopsy. Results in 7 definite and 45 possible carriers of Duchenne muscular dystrophy
C Doriguzzi, L Palmucci, T Mongini, et al.
Minerva Medica
|
September 15, 1980
[Progressive muscular dystrophy of the Duchenne type. Epidemiology and strategy for prevention]
C Doriguzzi, A Bertolotto, T Mongini, et al.
Italian Journal of Orthopaedics and Traumatology
|
December 1, 1984
Histomorphometric study of the dynamics of mineralization in a case of osteomalacia caused by anticonvulsants treated with 25(OH)d3
M Portigliatti Barbos, P Rossi, A Jeantet, et al.
European Journal of Histochemistry : EJH
|
January 1, 1994
Metachromatic dye-Ca++ATPase method in pathological muscle: a study of 382 muscle biopsies
C Doriguzzi, L Palmucci, T Mongini, et al.
Acta Neuropathologica
|
January 1, 1990
Cytochrome c oxidase and coenzyme Q in neuromuscular diseases: a histochemical study
C Doriguzzi, L Palmucci, B Pollo, et al.
Page
of 6