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Journal of Inherited Metabolic Disease
|
June 16, 2007
Upper airway obstructive disease in mucopolysaccharidoses: polysomnography, computed tomography and nasal endoscopy findings
F Santamaria, M V Andreucci, G Parenti, et al.
American Journal of Respiratory and Critical Care Medicine
|
February 1, 1996
Early detection of lung involvement in lysinuric protein intolerance: role of high-resolution computed tomography and radioisotopic methods
F Santamaria, G Parenti, G Guidi, et al.
European Journal of Pediatrics
|
December 11, 2008
Vitamin E supplementation improves neutropenia and reduces the frequency of infections in patients with glycogen storage disease type 1b
D Melis, R Della Casa, R Parini, et al.
Human Mutation
|
June 29, 2004
Screening of 25 Italian patients with Niemann-Pick A reveals fourteen new mutations, one common and thirteen private, in SMPD1
V Ricci, M Stroppiano, F Corsolini, et al.
Minerva Pediatrica
|
September 21, 2012
Epilepsy in inherited metabolic disorders: a pediatric series
G Vitiello, V De Clemente, R Della Casa, et al.
FEBS Letters
|
October 22, 1998
Structure and mutation analysis of the glycogen storage disease type 1b gene
P Marcolongo, V Barone, G Priori, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 27, 2011
Developmental evolution in a patient with multiple acyl-coenzymeA dehydrogenase deficiency under pharmacological treatment
M Rosa, A Pascarella, G Parenti, et al.
Journal of Endocrinological Investigation
|
April 14, 2006
Multi-step approach in a complex case of Cushing's syndrome and medullary thyroid carcinoma
G Parenti, R Nassi, S Silvestri, et al.
Journal of Inherited Metabolic Disease
|
April 26, 2008
Myasthenia gravis in a patient affected by glycogen storage disease type Ib: a further manifestation of an increased risk for autoimmune disorders?
D Melis, F Balivo, R Della Casa, et al.
The Neuroradiology Journal
|
November 22, 2013
Type a niemann-pick disease. Description of three cases with delayed myelination
A D'Amico, M Sibilio, F Caranci, et al.
Page
of 23
Search research articles
Search
Showing results (181-190 of 226) with videos related to
Sort By:
Page
of 23
Journal of Inherited Metabolic Disease
|
June 16, 2007
Upper airway obstructive disease in mucopolysaccharidoses: polysomnography, computed tomography and nasal endoscopy findings
F Santamaria, M V Andreucci, G Parenti, et al.
American Journal of Respiratory and Critical Care Medicine
|
February 1, 1996
Early detection of lung involvement in lysinuric protein intolerance: role of high-resolution computed tomography and radioisotopic methods
F Santamaria, G Parenti, G Guidi, et al.
European Journal of Pediatrics
|
December 11, 2008
Vitamin E supplementation improves neutropenia and reduces the frequency of infections in patients with glycogen storage disease type 1b
D Melis, R Della Casa, R Parini, et al.
Human Mutation
|
June 29, 2004
Screening of 25 Italian patients with Niemann-Pick A reveals fourteen new mutations, one common and thirteen private, in SMPD1
V Ricci, M Stroppiano, F Corsolini, et al.
Minerva Pediatrica
|
September 21, 2012
Epilepsy in inherited metabolic disorders: a pediatric series
G Vitiello, V De Clemente, R Della Casa, et al.
FEBS Letters
|
October 22, 1998
Structure and mutation analysis of the glycogen storage disease type 1b gene
P Marcolongo, V Barone, G Priori, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 27, 2011
Developmental evolution in a patient with multiple acyl-coenzymeA dehydrogenase deficiency under pharmacological treatment
M Rosa, A Pascarella, G Parenti, et al.
Journal of Endocrinological Investigation
|
April 14, 2006
Multi-step approach in a complex case of Cushing's syndrome and medullary thyroid carcinoma
G Parenti, R Nassi, S Silvestri, et al.
Journal of Inherited Metabolic Disease
|
April 26, 2008
Myasthenia gravis in a patient affected by glycogen storage disease type Ib: a further manifestation of an increased risk for autoimmune disorders?
D Melis, F Balivo, R Della Casa, et al.
The Neuroradiology Journal
|
November 22, 2013
Type a niemann-pick disease. Description of three cases with delayed myelination
A D'Amico, M Sibilio, F Caranci, et al.
Page
of 23