arginine and Congenital Disorders of Glycosylation

arginine has been researched along with Congenital Disorders of Glycosylation in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Aronica, E; Poll-The, BT; Rozemuller-Kwakkel, JM; Troost, D; van der Heide, M; van Kempen, AA; van Slooten, HJ	1
Appleton, D; Coman, D; Jaeken, J; Klingberg, S; MacDonald, R; McGill, J; Morris, D	1

Other Studies

2 other study(ies) available for arginine and Congenital Disorders of Glycosylation

Article	Year
Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology. Acta neuropathologica, 2005, Volume: 109, Issue:4 Topics: Arginine; Atrophy; Calbindins; Cerebellum; Congenital Disorders of Glycosylation; DNA Mutational Analysis; Humans; Immunohistochemistry; Infant, Newborn; Male; Methionine; Microscopy, Electron, Transmission; Muscle, Skeletal; Mutation; Neuroglia; Neurons; Phosphotransferases (Phosphomutases); S100 Calcium Binding Protein G; Threonine; Valine; Vimentin	2005
Congenital disorder of glycosylation type 1a: three siblings with a mild neurological phenotype. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2007, Volume: 14, Issue:7 Topics: Adult; Arginine; Ataxia; Cerebellar Diseases; Congenital Disorders of Glycosylation; Female; Histidine; Humans; Intellectual Disability; Lysine; Magnetic Resonance Imaging; Male; Mutation; Osteoporosis; Phenotype; Phosphotransferases (Phosphomutases); Siblings	2007

Article

Year

Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology.

Acta neuropathologica, 2005, Volume: 109, Issue:4

Topics: Arginine; Atrophy; Calbindins; Cerebellum; Congenital Disorders of Glycosylation; DNA Mutational Analysis; Humans; Immunohistochemistry; Infant, Newborn; Male; Methionine; Microscopy, Electron, Transmission; Muscle, Skeletal; Mutation; Neuroglia; Neurons; Phosphotransferases (Phosphomutases); S100 Calcium Binding Protein G; Threonine; Valine; Vimentin

2005

Congenital disorder of glycosylation type 1a: three siblings with a mild neurological phenotype.

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2007, Volume: 14, Issue:7

Topics: Adult; Arginine; Ataxia; Cerebellar Diseases; Congenital Disorders of Glycosylation; Female; Histidine; Humans; Intellectual Disability; Lysine; Magnetic Resonance Imaging; Male; Mutation; Osteoporosis; Phenotype; Phosphotransferases (Phosphomutases); Siblings

2007