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JIMD Reports
|
February 23, 2013
COG5-CDG with a Mild Neurohepatic Presentation
C W Fung, G Matthijs, L Sturiale, et al.
Italian Journal of Neurological Sciences
|
September 1, 1994
Brachial plexus injuries. Guidelines for management: our experience
S Ferraresi, D Garozzo, C Griffini, et al.
Journal of Inherited Metabolic Disease
|
December 11, 2008
Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation (CDG) type IIx
P L Calvo, S Pagliardini, M Baldi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 22, 2007
Clinical and biochemical features in a Congolese infant with congenital disorder of glycosylation (CDG)-IIx
N C Nsibu, J Jaeken, H Carchon, et al.
Journal of Mass Spectrometry : JMS
|
April 27, 2017
MALDI-MS profiling of serum O-glycosylation and N-glycosylation in COG5-CDG
A Palmigiano, R O Bua, R Barone, et al.
JIMD Reports
|
February 23, 2013
Deficiency of Subunit 6 of the Conserved Oligomeric Golgi Complex (COG6-CDG): Second Patient, Different Phenotype
S Huybrechts, C De Laet, P Bontems, et al.
JIMD Reports
|
February 23, 2013
Two Argentinean Siblings with CDG-Ix: A Novel Type of Congenital Disorder of Glycosylation?
M B Bistué Millón, M A Delgado, N B Azar, et al.
Journal of Neurology
|
October 31, 2014
A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation
Rita Barone, M Carrozzi, R Parini, et al.
Frontiers in Surgery
|
July 15, 2022
Women in Neurosurgery: Historical Path to Self-Segregation and Proposal for an Integrated Future
D Garozzo, R Rispoli, F Graziano, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 29 results.
JIMD Reports
|
February 23, 2013
COG5-CDG with a Mild Neurohepatic Presentation
C W Fung, G Matthijs, L Sturiale, et al.
Italian Journal of Neurological Sciences
|
September 1, 1994
Brachial plexus injuries. Guidelines for management: our experience
S Ferraresi, D Garozzo, C Griffini, et al.
Journal of Inherited Metabolic Disease
|
December 11, 2008
Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation (CDG) type IIx
P L Calvo, S Pagliardini, M Baldi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 22, 2007
Clinical and biochemical features in a Congolese infant with congenital disorder of glycosylation (CDG)-IIx
N C Nsibu, J Jaeken, H Carchon, et al.
Journal of Mass Spectrometry : JMS
|
April 27, 2017
MALDI-MS profiling of serum O-glycosylation and N-glycosylation in COG5-CDG
A Palmigiano, R O Bua, R Barone, et al.
JIMD Reports
|
February 23, 2013
Deficiency of Subunit 6 of the Conserved Oligomeric Golgi Complex (COG6-CDG): Second Patient, Different Phenotype
S Huybrechts, C De Laet, P Bontems, et al.
JIMD Reports
|
February 23, 2013
Two Argentinean Siblings with CDG-Ix: A Novel Type of Congenital Disorder of Glycosylation?
M B Bistué Millón, M A Delgado, N B Azar, et al.
Journal of Neurology
|
October 31, 2014
A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation
Rita Barone, M Carrozzi, R Parini, et al.
Frontiers in Surgery
|
July 15, 2022
Women in Neurosurgery: Historical Path to Self-Segregation and Proposal for an Integrated Future
D Garozzo, R Rispoli, F Graziano, et al.
Page
of 3