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European Journal of Pediatrics
|
May 1, 1990
A new therapeutic approach for X-linked adrenoleukodystrophy
M Cappa, E Bertini, M Di Capua, et al.
Developmental Medicine and Child Neurology
|
December 1, 1994
Early cognition, communication and language in children with focal brain injury
A M Dall'Oglio, E Bates, V Volterra, et al.
Journal of Child Neurology
|
August 21, 2001
Neurofibromatosis type 1 presenting with hand dystonia
M Di Capua, M L Lispi, A Giannotti, et al.
Epilepsy Research. Supplement
|
January 1, 1992
Sixth-month benign familial convulsions
F Vigevano, M Di Capua, L Fusco, et al.
European Journal of Pediatrics
|
August 1, 1992
Benign infantile familial convulsions
F Vigevano, L Fusco, M Di Capua, et al.
Neuropediatrics
|
February 1, 1994
Bilateral, reversible, selective thalamic involvement demonstrated by brain MR and acute severe neurological dysfunction with favorable outcome
R Cusmai, E Bertini, M Di Capua, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 22, 2000
Familial spastic paraplegia, axonal sensory-motor polyneuropathy and bulbar amyotrophy with facial dysmorphia: new cases of Troyer-like syndrome
E Bertini, M Sabatelli, M Di Capua, et al.
American Journal of Medical Genetics
|
July 1, 1989
Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: a variant of infantile spinal muscular atrophy
E Bertini, J L Gadisseux, G Palmieri, et al.
Biochemical and Biophysical Research Communications
|
May 8, 1998
A novel insertion mutation (A169i) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient
F M Santorelli, E Bertini, V Petruzzella, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
October 23, 2009
Cost of care of haemophilia with inhibitors
M N D Di Minno, G Di Minno, M Di Capua, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
European Journal of Pediatrics
|
May 1, 1990
A new therapeutic approach for X-linked adrenoleukodystrophy
M Cappa, E Bertini, M Di Capua, et al.
Developmental Medicine and Child Neurology
|
December 1, 1994
Early cognition, communication and language in children with focal brain injury
A M Dall'Oglio, E Bates, V Volterra, et al.
Journal of Child Neurology
|
August 21, 2001
Neurofibromatosis type 1 presenting with hand dystonia
M Di Capua, M L Lispi, A Giannotti, et al.
Epilepsy Research. Supplement
|
January 1, 1992
Sixth-month benign familial convulsions
F Vigevano, M Di Capua, L Fusco, et al.
European Journal of Pediatrics
|
August 1, 1992
Benign infantile familial convulsions
F Vigevano, L Fusco, M Di Capua, et al.
Neuropediatrics
|
February 1, 1994
Bilateral, reversible, selective thalamic involvement demonstrated by brain MR and acute severe neurological dysfunction with favorable outcome
R Cusmai, E Bertini, M Di Capua, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 22, 2000
Familial spastic paraplegia, axonal sensory-motor polyneuropathy and bulbar amyotrophy with facial dysmorphia: new cases of Troyer-like syndrome
E Bertini, M Sabatelli, M Di Capua, et al.
American Journal of Medical Genetics
|
July 1, 1989
Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: a variant of infantile spinal muscular atrophy
E Bertini, J L Gadisseux, G Palmieri, et al.
Biochemical and Biophysical Research Communications
|
May 8, 1998
A novel insertion mutation (A169i) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient
F M Santorelli, E Bertini, V Petruzzella, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
October 23, 2009
Cost of care of haemophilia with inhibitors
M N D Di Minno, G Di Minno, M Di Capua, et al.
Page
of 4