Page last updated: 2024-08-23

transferrin and Encephalomyopathies, Mitochondrial

transferrin has been researched along with Encephalomyopathies, Mitochondrial in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Artigas, J; Briones, P; Chabás, A; Colomer, J; Ferrer, I; García-Silva, MT; Jaeken, J; Pineda, M; Vilaseca, MA	1

Other Studies

1 other study(ies) available for transferrin and Encephalomyopathies, Mitochondrial

Article	Year
Congenital disorders of glycosylation (CDG) may be underdiagnosed when mimicking mitochondrial disease. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2001, Volume: 5, Issue:3 Topics: Acidosis, Lactic; Adolescent; Adult; Child, Preschool; Consanguinity; Diagnosis, Differential; DNA Mutational Analysis; Female; Genetic Carrier Screening; Glycosylation; Humans; Leigh Disease; Male; Mitochondrial Encephalomyopathies; Phosphotransferases (Phosphomutases); Retinitis Pigmentosa; Spinocerebellar Degenerations; Transferrin	2001

Article

Year

Congenital disorders of glycosylation (CDG) may be underdiagnosed when mimicking mitochondrial disease.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2001, Volume: 5, Issue:3

Topics: Acidosis, Lactic; Adolescent; Adult; Child, Preschool; Consanguinity; Diagnosis, Differential; DNA Mutational Analysis; Female; Genetic Carrier Screening; Glycosylation; Humans; Leigh Disease; Male; Mitochondrial Encephalomyopathies; Phosphotransferases (Phosphomutases); Retinitis Pigmentosa; Spinocerebellar Degenerations; Transferrin

2001