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R Mostardini

Showing results (1-10 of 11) with videos related to

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Minerva Pediatrica|March 1, 1991
[Encephalomyopathy due to a beta oxidation deficiency. Report of a new case]P Balestri, R Mostardini
Brain & Development|January 1, 1987
Clinical experiences of petit malA Fois, F Malandrini, R Mostardini
Brain & Development|January 1, 1987
Further observations on the treatment of infantile spasms with corticotropinA Fois, F Malandrini, R Mostardini
Journal of Neurology|August 18, 2004
Brain mitochondrial impairment in ethylmalonic encephalopathySalvatore Grosso, Paolo Balestri, R Mostardini, et al.
Clinical Dysmorphology|October 25, 2000
MOMO syndrome: a possible third caseR Zannolli, R Mostardini, T Hadjistilianou, et al.
American Journal of Medical Genetics|December 5, 2000
Char syndrome: an additional family with polythelia, a new findingR Zannolli, R Mostardini, M Matera, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 1, 1994
Vigabatrin treatment in childrenA Fois, S Buoni, R M Di Bartolo, et al.
Pediatric Dermatology|September 29, 2001
Cranioectodermal dysplasia: a new patient with an inapparent, subtle phenotypeR Zannolli, R Mostardini, M L Carpentieri, et al.
Seizure|March 31, 2005
Efficacy and safety of topiramate in infants according to epilepsy syndromesS Grosso, D Galimberti, M A Farnetani, et al.
American Journal of Medical Genetics|July 27, 2001
Corpus callosum agenesis, multiple cysts, skin defects, and subtle ocular abnormalities with a de novo mutation [45,XX,der(5), t(5;;14) (pter;q11.2)]R Zannolli, R Mostardini, L Pucci, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Minerva Pediatrica|March 1, 1991
[Encephalomyopathy due to a beta oxidation deficiency. Report of a new case]P Balestri, R Mostardini
Brain & Development|January 1, 1987
Clinical experiences of petit malA Fois, F Malandrini, R Mostardini
Brain & Development|January 1, 1987
Further observations on the treatment of infantile spasms with corticotropinA Fois, F Malandrini, R Mostardini
Journal of Neurology|August 18, 2004
Brain mitochondrial impairment in ethylmalonic encephalopathySalvatore Grosso, Paolo Balestri, R Mostardini, et al.
Clinical Dysmorphology|October 25, 2000
MOMO syndrome: a possible third caseR Zannolli, R Mostardini, T Hadjistilianou, et al.
American Journal of Medical Genetics|December 5, 2000
Char syndrome: an additional family with polythelia, a new findingR Zannolli, R Mostardini, M Matera, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 1, 1994
Vigabatrin treatment in childrenA Fois, S Buoni, R M Di Bartolo, et al.
Pediatric Dermatology|September 29, 2001
Cranioectodermal dysplasia: a new patient with an inapparent, subtle phenotypeR Zannolli, R Mostardini, M L Carpentieri, et al.
Seizure|March 31, 2005
Efficacy and safety of topiramate in infants according to epilepsy syndromesS Grosso, D Galimberti, M A Farnetani, et al.
American Journal of Medical Genetics|July 27, 2001
Corpus callosum agenesis, multiple cysts, skin defects, and subtle ocular abnormalities with a de novo mutation [45,XX,der(5), t(5;;14) (pter;q11.2)]R Zannolli, R Mostardini, L Pucci, et al.
Pageof 2