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L Morandi

Showing results (51-60 of 101) with videos related to

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Journal of Inherited Metabolic Disease|January 27, 2005
Severe neonatal onset of glycogenosis type IV: clinical and laboratory findings leading to diagnosis in two siblingsB Giuffrè, R Parini, T Rizzuti, et al.
Histopathology|December 21, 2002
Fibrinogen storage disease without hypofibrinogenaemia associated with acute infectionG Marucci, L Morandi, S Macchia, et al.
Annals of Neurology|June 14, 2000
Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositisC Di Blasi, M Mora, D Pareyson, et al.
Journal of the Neurological Sciences|October 1, 1995
Dystrophin characterization in BMD patients: correlation of abnormal protein with clinical phenotypeL Morandi, M Mora, V Confalonieri, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 1, 1988
Adjuvant chemotherapy with vincristine, cyclophosphamide, and doxorubicin after radiotherapy in local-regional nasopharyngeal cancer: results of a 4-year multicenter randomized studyA Rossi, R Molinari, P Boracchi, et al.
Histology and Histopathology|November 18, 2008
Genetic and molecular alterations in rhabdomyosarcoma: mRNA overexpression of MCL1 and MAP2K4 genesL Pazzaglia, A Chiechi, A Conti, et al.
European Journal of Gastroenterology & Hepatology|May 20, 1999
Detection of Helicobacter pylori cagA gene by polymerase chain reaction in faecal samplesF Russo, M Notarnicola, G Di Matteo, et al.
Muscle & Nerve|October 1, 1994
Fetus-like dystrophin expression and other cytoskeletal protein abnormalities in centronuclear myopathiesM Mora, L Morandi, L Merlini, et al.
American Journal of Medical Genetics|December 4, 1995
DMD and BMD in the same family due to distinct mutationsL Morandi, M Mora, S Tedeschi, et al.
Acta Neurologica Scandinavica|May 18, 2013
No evidence of cardiomyopathy in spinal and bulbar muscular atrophyG Querin, P Melacini, C D'Ascenzo, et al.
Pageof 11

Showing results (51-60 of 101) with videos related to

Sort By:
Pageof 11
Journal of Inherited Metabolic Disease|January 27, 2005
Severe neonatal onset of glycogenosis type IV: clinical and laboratory findings leading to diagnosis in two siblingsB Giuffrè, R Parini, T Rizzuti, et al.
Histopathology|December 21, 2002
Fibrinogen storage disease without hypofibrinogenaemia associated with acute infectionG Marucci, L Morandi, S Macchia, et al.
Annals of Neurology|June 14, 2000
Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositisC Di Blasi, M Mora, D Pareyson, et al.
Journal of the Neurological Sciences|October 1, 1995
Dystrophin characterization in BMD patients: correlation of abnormal protein with clinical phenotypeL Morandi, M Mora, V Confalonieri, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 1, 1988
Adjuvant chemotherapy with vincristine, cyclophosphamide, and doxorubicin after radiotherapy in local-regional nasopharyngeal cancer: results of a 4-year multicenter randomized studyA Rossi, R Molinari, P Boracchi, et al.
Histology and Histopathology|November 18, 2008
Genetic and molecular alterations in rhabdomyosarcoma: mRNA overexpression of MCL1 and MAP2K4 genesL Pazzaglia, A Chiechi, A Conti, et al.
European Journal of Gastroenterology & Hepatology|May 20, 1999
Detection of Helicobacter pylori cagA gene by polymerase chain reaction in faecal samplesF Russo, M Notarnicola, G Di Matteo, et al.
Muscle & Nerve|October 1, 1994
Fetus-like dystrophin expression and other cytoskeletal protein abnormalities in centronuclear myopathiesM Mora, L Morandi, L Merlini, et al.
American Journal of Medical Genetics|December 4, 1995
DMD and BMD in the same family due to distinct mutationsL Morandi, M Mora, S Tedeschi, et al.
Acta Neurologica Scandinavica|May 18, 2013
No evidence of cardiomyopathy in spinal and bulbar muscular atrophyG Querin, P Melacini, C D'Ascenzo, et al.
Pageof 11