Compounds > transferrin
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transferrin and Amenorrhea

transferrin has been researched along with Amenorrhea in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19902 (40.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Rojas-Roldan, L; Wilkins, T1
Michel, H1
North, JD; Scott, PJ; Wilson, JD1
Beutler, E; Fairbanks, VF; Fernandez, MA; Gelbart, T; Lee, P; Trevino, R1
Andersen, CH; Dreyer, V; Freiesleben, E; Gürtler, H; Hauge, M; Kissmeyer-Nielsen, F; Nielsen, LS; Pers, M; Philip, J; Robson, EB; Sorensen, B; Svejgaard, A1

Other Studies

5 other study(ies) available for transferrin and Amenorrhea

ArticleYear
Fatigue, arthralgia, amenorrhea--Dx?
    The Journal of family practice, 2014, Volume: 63, Issue:6

    Topics: Alanine Transaminase; Alkaline Phosphatase; Amenorrhea; Arthralgia; Aspartate Aminotransferases; Fatigue; Fatty Liver; Female; Ferritins; Gallstones; Genotype; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Iron; Membrane Proteins; Middle Aged; Mutation; Portal Vein; Splenomegaly; Transferrin; Ultrasonography

2014
[Hereditary hemochromatosis].
    Soins; la revue de reference infirmiere, 2007, Issue:716

    Topics: Age Distribution; Amenorrhea; Arrhythmias, Cardiac; Arthralgia; Erectile Dysfunction; Fatigue; Female; France; Genetic Testing; Hemochromatosis; Humans; Intestinal Absorption; Iron; Liver Cirrhosis; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Public Health; Transferrin

2007
Hemochromatosis in association with hereditary spherocyto- sis.
    Archives of internal medicine, 1967, Volume: 120, Issue:6

    Topics: Adult; Amenorrhea; Female; Hemochromatosis; Humans; Liver Cirrhosis; Pigmentation Disorders; Punctures; Spherocytosis, Hereditary; Splenectomy; Transferrin; Veins

1967
Molecular characterization of a case of atransferrinemia.
    Blood, 2000, Dec-15, Volume: 96, Issue:13

    Topics: Adult; Amenorrhea; Amino Acid Substitution; Anemia; Combined Modality Therapy; DNA Mutational Analysis; DNA, Complementary; Exons; Female; Gene Duplication; Humans; Hypothyroidism; Illinois; Introns; Iron; Iron Overload; Mutagenesis, Insertional; Osteoporosis; Phlebotomy; Plasma; Recurrence; Sequence Deletion; Transferrin

2000
Colour vision deficiency in on of two presumably monozygotic twins with secondary amenorrhoea.
    Annals of human genetics, 1969, Volume: 33, Issue:2

    Topics: Adolescent; Adult; Amenorrhea; Blood Group Antigens; Child; Child, Preschool; Color Vision Defects; Dermatoglyphics; Diseases in Twins; Erythrocytes; Female; Haptoglobins; Histocompatibility Testing; Humans; Karyotyping; Skin Transplantation; Transferrin; Transplantation, Homologous

1969