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HEREDITARY / CONGENITAL DISEASES OR DISORDERS

Exhibiting 206 entries found in the GMN corpus.

YearTitle & TagsAuthor(s)
1938 CEIcterus gravis (erythroblastosis) neonatorum.
1909 CEInborn errors of metabolism.
1958 CEInfluence of light on the hyperbilirubinaemia of infants.
1933 CEInherited abnormalities of the skin and its appendages.
1861 CEKlinik der Leberkrankheiten. Bd. 2.
1894 CEKlinische Abbildungen: Sammlung von Darstellungen der Veränderung der äusseren Körperform bei inneren Krankheiten.
1958 CEL’Hérédité en ophtalmologie.
1886 CELa syphilis héréditaire tardive.
1899 CELe trophoedème chronique héréditaire.
1883 CE​–1884 CELehrbuch der speciellen Pathologie und Therapie der inneren Krankheiten. 2 vols.
1959 CELes cataractes congénitales.
1904 CELes scolioses congénitales.
1519 CELiber theoricae nec non practicae Alsaharavii.
1859 CELieber das Alcapton; ein neuer Beitrag zur Frage: welche Stoffe des Harns können Kupferreduction bewirken?
1907 CELigation of the ductus arteriosus.
1990 CELinkage of early-onset familial breast cancer to Chromosome 17q21.
1994 CELocation of a breast cancer susceptibility gene, BRACA2, to chromosome 13q12-13.
1966 CEMan’s haemoglobins: including the haemoglobinopathies and their investigation.
1936 CEMediterranean disease – thalassemia (erythroblastic anemia of Cooley); associated pigment abnormalities simulating hemochromatosis.
1803 CEMemoria chirurgica sui piedi torti congenita dei fanciulli.
1831 CEMerkwürdige Fragilität der Knochen ohne dyskrasische Ursache als krankhafte Eigenthümlichkeit dreier Geschwister.
1968 CEMolecular pathology of human haemoglobin.
1928 CEMongolism. A study of the physical and mental characteristics of mongolian imbeciles. Revised by H. G. Brainerd.
1832 CEMonographie des dermatoses.
1971 CEMutation and cancer: Statistical study of retinoblastoma.
1923 CENouvelle observation d’acrocéphalosyndactylie.
1798 CEObservation sur un enfant né sans anus, et auquel il a été fait une ouverture pour y suppléer.
1866 CEObservations on an ethnic classification of idiots.
1874 CEOm den medfödda, färgblindhetens diagnostic och teori.
1876 CE​–1877 CEOm färgblindheten i dess förhallande till jernvägstrafiken och sjöväsendet.
1887 CEOn arrested cerebral development, with special reference to its cortical pathology.
1879 CEOn astigmatism as a cause for persistent headache and other nervous symptoms.
1872 CEOn chorea.
1810 CEOn cystic oxide, a new species of urinary calculus.
1876 CE​–1877 CEOn irregular and defective tooth development.
1839 CEOn the nature of club-foot and analogous distortions.
1878 CEOn the treatment of psoriasis by an ointment of chrysophanic acid.
1839 CEOperations on club-feet.
1949 CEOsteogenesis imperfecta: A study of clinical features and heredity based on 55 Danish families comprising 180 affected members.
1967 CEOsteotomies totales de la face: Syndrome de Crouzon, syndrome d'Apert: oxcephalies, scaphocephalies, turricephalies.
1814 CEPathological researches. Essay I. On malformations of the human heart. [All published.]
1910 CEPeculiar elongated and sickle-shaped red blood corpuscles in a case of severe anemia.
Periodic Disease: A probable syndrome including periodic fever, benign paroxysmal peritonitis, cyclic neutropenia and intermittent arthralgia.
1842 CEPractice of medicine: A treatise on special pathology and therapeutics. 2 vols.
1922 CEPremature and congenitally diseased infants.
1939 CEPrinciples involved in the treatment of congenital clubfoot.
1954 CEProtection afforded by sickle-cell trait against subtertian malarial infection.
1948 CEPulmonary valvulotomy for the relief of congenital pulmonary stenosis. Report of three cases.
1827 CERecherches sur l’agénésie cérébrale et la paralysie congénitale.
1938 CERecherches sur l’anémie érythroblastique infantile des peuples de la Méditerranée orientale. Étude anthropologique, étiologique et pathogénique. La transmission héréditaire de la maladie.