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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 24, 2018
A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype
Giulia Iapadre, Giovanni Morana, Maria Stella Vari, et al.
Epilepsy & Behavior : E&B
|
May 25, 2025
Exploring neurodevelopment in CDKL5 deficiency disorder: Current insights and future directions
Giovanni Battista Dell'Isola, Martina Giorgia Perinelli, Alessia Frulli, et al.
Current Neuropharmacology
|
December 2, 2010
Clinical and pharmacological aspects of inflammatory demyelinating diseases in childhood: an update
Alberto Spalice, Pasquale Parisi, Laura Papetti, et al.
International Journal of Endocrinology
|
August 10, 2017
Central Precocious Puberty and Response to GnRHa Therapy in Children with Cerebral Palsy and Moderate to Severe Motor Impairment: Data from a Longitudinal, Case-Control, Multicentre, Italian Study
Patrizia Bruzzi, Maria Francesca Messina, Alessandra Bartoli, et al.
Hormones (Athens, Greece)
|
July 11, 2016
Bone mineral status and metabolism in patients with Williams-Beuren syndrome
Stefano Stagi, Cristina Manoni, Perla Scalini, et al.
SAGE Open Medical Case Reports
|
May 30, 2023
Acute lymphoblastic leukemia relapse presenting with optic nerve infiltration
Gianluca Dini, Ilaria Capolsini, Carla Cerri, et al.
Italian Journal of Pediatrics
|
July 19, 2022
Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus
Antonella Riva, Elisabetta Amadori, Maria Stella Vari, et al.
Minerva Pediatrica
|
April 15, 2016
Association among nocturnal enuresis, body weight and obstructive sleep apnea in children of south Italy: an observational study
Pietro Ferrara, Giovanna C Fabrizio, Daniele Franco, et al.
Clinical Rheumatology
|
September 16, 2017
Macrophage activation syndrome in Still's disease: analysis of clinical characteristics and survival in paediatric and adult patients
Piero Ruscitti, Carmela Rago, Luciana Breda, et al.
Cytogenetic and Genome Research
|
September 7, 2017
X-Linked Hypohidrotic Ectodermal Dysplasia: New Features and a Novel EDA Gene Mutation
Salvatore Savasta, Giorgia Carlone, Riccardo Castagnoli, et al.
Page
of 45
Search research articles
Search
Showing results (321-330 of 448) with videos related to
Sort By:
Page
of 45
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 24, 2018
A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype
Giulia Iapadre, Giovanni Morana, Maria Stella Vari, et al.
Epilepsy & Behavior : E&B
|
May 25, 2025
Exploring neurodevelopment in CDKL5 deficiency disorder: Current insights and future directions
Giovanni Battista Dell'Isola, Martina Giorgia Perinelli, Alessia Frulli, et al.
Current Neuropharmacology
|
December 2, 2010
Clinical and pharmacological aspects of inflammatory demyelinating diseases in childhood: an update
Alberto Spalice, Pasquale Parisi, Laura Papetti, et al.
International Journal of Endocrinology
|
August 10, 2017
Central Precocious Puberty and Response to GnRHa Therapy in Children with Cerebral Palsy and Moderate to Severe Motor Impairment: Data from a Longitudinal, Case-Control, Multicentre, Italian Study
Patrizia Bruzzi, Maria Francesca Messina, Alessandra Bartoli, et al.
Hormones (Athens, Greece)
|
July 11, 2016
Bone mineral status and metabolism in patients with Williams-Beuren syndrome
Stefano Stagi, Cristina Manoni, Perla Scalini, et al.
SAGE Open Medical Case Reports
|
May 30, 2023
Acute lymphoblastic leukemia relapse presenting with optic nerve infiltration
Gianluca Dini, Ilaria Capolsini, Carla Cerri, et al.
Italian Journal of Pediatrics
|
July 19, 2022
Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus
Antonella Riva, Elisabetta Amadori, Maria Stella Vari, et al.
Minerva Pediatrica
|
April 15, 2016
Association among nocturnal enuresis, body weight and obstructive sleep apnea in children of south Italy: an observational study
Pietro Ferrara, Giovanna C Fabrizio, Daniele Franco, et al.
Clinical Rheumatology
|
September 16, 2017
Macrophage activation syndrome in Still's disease: analysis of clinical characteristics and survival in paediatric and adult patients
Piero Ruscitti, Carmela Rago, Luciana Breda, et al.
Cytogenetic and Genome Research
|
September 7, 2017
X-Linked Hypohidrotic Ectodermal Dysplasia: New Features and a Novel EDA Gene Mutation
Salvatore Savasta, Giorgia Carlone, Riccardo Castagnoli, et al.
Page
of 45