Page last updated: 2024-08-23

transferrin and Brachial Paresis

transferrin has been researched along with Brachial Paresis in 1 studies

Research

Studies (1)

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

Authors

Authors	Studies
Knauer, R; Körner, C; Lehle, L; Marquardt, T; Stephani, U; von Figura, K	1

Other Studies

1 other study(ies) available for transferrin and Brachial Paresis

Article	Year
Carbohydrate deficient glycoprotein syndrome type IV: deficiency of dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase. The EMBO journal, 1999, Dec-01, Volume: 18, Issue:23 Topics: Amino Acid Sequence; Carboxypeptidases; Cathepsin A; Child, Preschool; Congenital Disorders of Glycosylation; DNA Mutational Analysis; Endoplasmic Reticulum; Genetic Complementation Test; Glycosylation; Humans; Male; Mannosyltransferases; Molecular Sequence Data; Mutation, Missense; Paresis; Sequence Homology, Amino Acid; Time Factors; Transferrin	1999

Article

Year

Carbohydrate deficient glycoprotein syndrome type IV: deficiency of dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase.

The EMBO journal, 1999, Dec-01, Volume: 18, Issue:23

Topics: Amino Acid Sequence; Carboxypeptidases; Cathepsin A; Child, Preschool; Congenital Disorders of Glycosylation; DNA Mutational Analysis; Endoplasmic Reticulum; Genetic Complementation Test; Glycosylation; Humans; Male; Mannosyltransferases; Molecular Sequence Data; Mutation, Missense; Paresis; Sequence Homology, Amino Acid; Time Factors; Transferrin

1999