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Hormone Research in Paediatrics
|
January 10, 2014
Impaired bone metabolism in glycogen storage disease type 1 is associated with poor metabolic control in type 1a and with granulocyte colony-stimulating factor therapy in type 1b
D Melis, R Pivonello, M Cozzolino, et al.
Clinical Endocrinology
|
June 21, 2005
Efficacy of ACE-inhibitor therapy on renal disease in glycogen storage disease type 1: a multicentre retrospective study
D Melis, G Parenti, R Gatti, et al.
Human Mutation
|
April 23, 2008
Molecular and functional characterization of eight novel GAA mutations in Italian infants with Pompe disease
M G Pittis, M Donnarumma, A L E Montalvo, et al.
American Journal of Human Genetics
|
January 13, 2000
Structure of the SLC7A7 gene and mutational analysis of patients affected by lysinuric protein intolerance
M P Sperandeo, M T Bassi, M Riboni, et al.
Journal of the American College of Radiology : JACR
|
May 26, 2023
ACR Appropriateness Criteria® Workup of Noncerebral Systemic Arterial Embolic Source
, Vincent G Parenti, Kanupriya Vijay, et al.
Journal of Endocrinological Investigation
|
November 21, 2017
Approach to hyponatremia according to the clinical setting: Consensus statement from the Italian Society of Endocrinology (SIE), Italian Society of Nephrology (SIN), and Italian Association of Medical Oncology (AIOM)
E Sbardella, A M Isidori, G Arnaldi, et al.
Page
of 23
Search research articles
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Showing results (221-230 of 226) with videos related to
Sort By:
Page
of 23
You have reached the last page of results.
This site can display upto 226 results.
Hormone Research in Paediatrics
|
January 10, 2014
Impaired bone metabolism in glycogen storage disease type 1 is associated with poor metabolic control in type 1a and with granulocyte colony-stimulating factor therapy in type 1b
D Melis, R Pivonello, M Cozzolino, et al.
Clinical Endocrinology
|
June 21, 2005
Efficacy of ACE-inhibitor therapy on renal disease in glycogen storage disease type 1: a multicentre retrospective study
D Melis, G Parenti, R Gatti, et al.
Human Mutation
|
April 23, 2008
Molecular and functional characterization of eight novel GAA mutations in Italian infants with Pompe disease
M G Pittis, M Donnarumma, A L E Montalvo, et al.
American Journal of Human Genetics
|
January 13, 2000
Structure of the SLC7A7 gene and mutational analysis of patients affected by lysinuric protein intolerance
M P Sperandeo, M T Bassi, M Riboni, et al.
Journal of the American College of Radiology : JACR
|
May 26, 2023
ACR Appropriateness Criteria® Workup of Noncerebral Systemic Arterial Embolic Source
, Vincent G Parenti, Kanupriya Vijay, et al.
Journal of Endocrinological Investigation
|
November 21, 2017
Approach to hyponatremia according to the clinical setting: Consensus statement from the Italian Society of Endocrinology (SIE), Italian Society of Nephrology (SIN), and Italian Association of Medical Oncology (AIOM)
E Sbardella, A M Isidori, G Arnaldi, et al.
Page
of 23