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Anales Espanoles De Pediatria
|
June 1, 1990
[Basal pulmonary function studies (FVC, FEV) in a selected child population]
J Sanz Ortega, A Martorell Aragonés, A Alvarez Angel, et al.
Anales Espanoles De Pediatria
|
May 1, 1990
[Repercussion of risk factors associated with the development of chronic bronchial pathology on pulmonary function in children]
J Sanz Ortega, A Martorell Aragonés, V Alvarez Angel, et al.
Revista De Neurologia
|
July 28, 2005
[Hereditary neuromuscular diseases in paediatrics. Our experience over the last 14 years]
J López-Pisón, V Rebage, A Baldellou-Vázquez, et al.
Revista De Neurologia
|
December 29, 2000
[Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA]
L Coelho-Miranda, A Playan, R Artuch, et al.
Annals of Neurology
|
October 17, 2001
Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan Gypsies
P K Thomas, L Kalaydjieva, B Youl, et al.
Atencion Primaria
|
March 18, 2009
[Child and adolescent programme]
F J Soriano Faura, O Cortes Rico, J J Delgado Domínguez, et al.
Neurology
|
June 27, 2002
Clinicopathological features of genetically confirmed Danon disease
K Sugie, A Yamamoto, K Murayama, et al.
Neuromuscular Disorders : NMD
|
January 20, 2016
Long-term follow-up in patients with congenital myasthenic syndrome due to RAPSN mutations
D Natera-de Benito, M Bestué, J J Vilchez, et al.
Neuromuscular Disorders : NMD
|
June 16, 2019
Salbutamol tolerability and efficacy in patients with spinal muscular atrophy type II
A L Frongia, D Natera-de Benito, C Ortez, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
February 6, 2004
[Epidemiology and burden of acute otitis media in Valencia (Spain)]
M Garcés-Sánchez, J Díez-Domingo, T Alvarez de Labiada, et al.
Page
of 17
Search research articles
Search
Showing results (151-160 of 164) with videos related to
Sort By:
Page
of 17
Anales Espanoles De Pediatria
|
June 1, 1990
[Basal pulmonary function studies (FVC, FEV) in a selected child population]
J Sanz Ortega, A Martorell Aragonés, A Alvarez Angel, et al.
Anales Espanoles De Pediatria
|
May 1, 1990
[Repercussion of risk factors associated with the development of chronic bronchial pathology on pulmonary function in children]
J Sanz Ortega, A Martorell Aragonés, V Alvarez Angel, et al.
Revista De Neurologia
|
July 28, 2005
[Hereditary neuromuscular diseases in paediatrics. Our experience over the last 14 years]
J López-Pisón, V Rebage, A Baldellou-Vázquez, et al.
Revista De Neurologia
|
December 29, 2000
[Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA]
L Coelho-Miranda, A Playan, R Artuch, et al.
Annals of Neurology
|
October 17, 2001
Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan Gypsies
P K Thomas, L Kalaydjieva, B Youl, et al.
Atencion Primaria
|
March 18, 2009
[Child and adolescent programme]
F J Soriano Faura, O Cortes Rico, J J Delgado Domínguez, et al.
Neurology
|
June 27, 2002
Clinicopathological features of genetically confirmed Danon disease
K Sugie, A Yamamoto, K Murayama, et al.
Neuromuscular Disorders : NMD
|
January 20, 2016
Long-term follow-up in patients with congenital myasthenic syndrome due to RAPSN mutations
D Natera-de Benito, M Bestué, J J Vilchez, et al.
Neuromuscular Disorders : NMD
|
June 16, 2019
Salbutamol tolerability and efficacy in patients with spinal muscular atrophy type II
A L Frongia, D Natera-de Benito, C Ortez, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
February 6, 2004
[Epidemiology and burden of acute otitis media in Valencia (Spain)]
M Garcés-Sánchez, J Díez-Domingo, T Alvarez de Labiada, et al.
Page
of 17