Compounds > fibrinogen
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fibrinogen and Abnormalities, Autosome

fibrinogen has been researched along with Abnormalities, Autosome in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19907 (87.50)18.7374
1990's1 (12.50)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Brommer, EJ; Gravesen, M; Haverkate, F; Hensen, A1
Humphries, SE1
Erickson, RP; Pickart, L; Thaler, MM1
Cruz, AC; Kant, JA; Kitchens, CS1
Lagrue, G; Vernant, JP1
Fickers, M; Speck, B1
Soskin, LS; Usol'tsev, AN1
Caen, J1

Reviews

2 review(s) available for fibrinogen and Abnormalities, Autosome

ArticleYear
Genetic regulation of fibrinogen.
    European heart journal, 1995, Volume: 16 Suppl A

    Topics: Cardiovascular Diseases; Chromosome Aberrations; Chromosome Mapping; Fibrinogen; Gene Expression Regulation; Humans; Polymorphism, Genetic; Smoking

1995
[Dysautonomic syndrome and its differential diagnosis (literature review)].
    Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1970, Volume: 70, Issue:11

    Topics: Acrodynia; Adolescent; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Diagnosis, Differential; Dysautonomia, Familial; Familial Mediterranean Fever; Fibrinogen; Humans; Neurologic Manifestations; Peritonitis; Pheochromocytoma; Racial Groups

1970

Other Studies

6 other study(ies) available for fibrinogen and Abnormalities, Autosome

ArticleYear
[Familial dysfibrinogenemia; fibrinogen Haarlem I and II].
    Nederlands tijdschrift voor geneeskunde, 1981, May-09, Volume: 125, Issue:19

    Topics: Adult; Afibrinogenemia; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Female; Fibrinogen; Fibrinogens, Abnormal; Genes, Dominant; Humans; Male; Middle Aged; Pedigree

1981
Serum protein synthesis in mutant mice with abnormal hepatic endoplasmic reticulum.
    Cytobios, 1976, Volume: 15, Issue:57

    Topics: Albinism; alpha-Fetoproteins; Animals; Blood Proteins; Chromosome Aberrations; Chromosome Deletion; Endoplasmic Reticulum; Fibrinogen; Liver; Mice; Serum Albumin

1976
A unique 7p/12q chromosomal abnormality associated with recurrent abortion and hypofibrinogenemia.
    Blood, 1987, Volume: 70, Issue:4

    Topics: Abortion, Habitual; Adult; Chromosome Aberrations; Chromosome Disorders; Female; Fibrinogen; Humans; Karyotyping; Pedigree; Pregnancy; Translocation, Genetic

1987
[Hereditary amyloidosis].
    La Nouvelle presse medicale, 1972, Oct-28, Volume: 1, Issue:38

    Topics: Amyloidosis; Chromosome Aberrations; Chromosome Disorders; Deafness; Familial Mediterranean Fever; Fibrinogen; Heart Failure; Humans; Joint Diseases; Neurologic Manifestations; Pain; Peripheral Nervous System Diseases; Peritonitis; Polyneuropathies; Portugal; Prognosis; Racial Groups; Skin Diseases; Thyroid Neoplasms

1972
Thrombocythaemia. Familial occurrence and transition into blastic crisis.
    Acta haematologica, 1974, Volume: 51, Issue:5

    Topics: Alkaline Phosphatase; Anemia, Aplastic; Blood Coagulation Tests; Bone Marrow Examination; Busulfan; Chromosome Aberrations; Female; Fibrinogen; Gastrointestinal Hemorrhage; Humans; Inclusion Bodies; Leukemia; Leukocytes; Male; Phosphorus Radioisotopes; Prothrombin Time; Thiotepa; Thrombocytosis

1974
[Thrombopathy and thrombasthenia].
    Schweizerische medizinische Wochenschrift, 1968, Oct-19, Volume: 98, Issue:42

    Topics: Adenine Nucleotides; Adenosine Triphosphate; Anemia, Myelophthisic; Blood Coagulation; Blood Platelet Disorders; Chromosome Aberrations; Chromosome Disorders; Collagen; Diagnosis, Differential; Fibrinogen; Humans; Leukemia, Myeloid; Thrombocytopenia; Uremia

1968