BIOMAT Database Logo BIOMAT Database Logo

[Contribution to Gardner's syndrome]. 1968

W Fuhrmann, and K H Kärcher, and H Pfeifer, and U W Schnyder

UI MeSH Term Description Entries
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009377 Multiple Endocrine Neoplasia A group of autosomal dominant diseases characterized by the combined occurrence of tumors involving two or more ENDOCRINE GLANDS that secrete PEPTIDE HORMONES or AMINES. These neoplasias are often benign but can be malignant. They are classified by the endocrine glands involved and the degree of aggressiveness. The two major forms are MEN1 and MEN2 with gene mutations on CHROMOSOME 11 and CHROMOSOME 10, respectively. Adenomatosis, Familial Endocrine,Endocrine Neoplasia, Multiple,Multiple Endocrine Neoplasia Syndrome,Neoplasia, Multiple Endocrine,Neoplasms, Multiple Endocrine,Adenomatosis, Multiple Endocrine,Familial Endocrine Adenomatosis,Multiple Endocrine Adenomatosis,Multiple Endocrine Adenopathy,Multiple Endocrine Neoplasia Syndromes,Multiple Endocrine Neoplasms,Adenomatoses, Familial Endocrine,Adenomatoses, Multiple Endocrine,Adenopathies, Multiple Endocrine,Adenopathy, Multiple Endocrine,Endocrine Adenomatoses, Familial,Endocrine Adenomatoses, Multiple,Endocrine Adenomatosis, Familial,Endocrine Adenomatosis, Multiple,Endocrine Adenopathies, Multiple,Endocrine Adenopathy, Multiple,Endocrine Neoplasms, Multiple,Familial Endocrine Adenomatoses,Multiple Endocrine Adenomatoses,Multiple Endocrine Adenopathies
D010016 Osteoma A benign tumor composed of bone tissue or a hard tumor of bonelike structure developing on a bone (homoplastic osteoma) or on other structures (heteroplastic osteoma). (From Dorland, 27th ed) Osteomas
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002869 Chromosome Aberrations Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS. Autosome Abnormalities,Cytogenetic Aberrations,Abnormalities, Autosome,Abnormalities, Chromosomal,Abnormalities, Chromosome,Chromosomal Aberrations,Chromosome Abnormalities,Cytogenetic Abnormalities,Aberration, Chromosomal,Aberration, Chromosome,Aberration, Cytogenetic,Aberrations, Chromosomal,Aberrations, Chromosome,Aberrations, Cytogenetic,Abnormalities, Cytogenetic,Abnormality, Autosome,Abnormality, Chromosomal,Abnormality, Chromosome,Abnormality, Cytogenetic,Autosome Abnormality,Chromosomal Aberration,Chromosomal Abnormalities,Chromosomal Abnormality,Chromosome Aberration,Chromosome Abnormality,Cytogenetic Aberration,Cytogenetic Abnormality
D004814 Epidermal Cyst Intradermal or subcutaneous saclike structure, the wall of which is stratified epithelium containing keratohyalin granules. Epidermoid Cyst,Pilar Cyst,Sebaceous Cyst,Cyst, Epidermal,Cyst, Epidermoid,Cyst, Pilar,Cyst, Sebaceous,Cysts, Epidermal,Cysts, Epidermoid,Cysts, Pilar,Cysts, Sebaceous,Epidermal Cysts,Epidermoid Cysts,Pilar Cysts,Sebaceous Cysts
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

W Fuhrmann, and K H Kärcher, and H Pfeifer, and U W Schnyder
[Gardner's syndrome. Radiography and clinical contribution].
May 1973, Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin,
W Fuhrmann, and K H Kärcher, and H Pfeifer, and U W Schnyder
[Gardner's syndrome].
October 1974, Rinsho hoshasen. Clinical radiography,
W Fuhrmann, and K H Kärcher, and H Pfeifer, and U W Schnyder
[Gardner's syndrome].
January 1977, Nihon rinsho. Japanese journal of clinical medicine,
W Fuhrmann, and K H Kärcher, and H Pfeifer, and U W Schnyder
[Gardner's syndrome].
January 1972, Lyon chirurgical,
W Fuhrmann, and K H Kärcher, and H Pfeifer, and U W Schnyder
[Gardner's syndrome].
January 1974, Archives belges de dermatologie,
W Fuhrmann, and K H Kärcher, and H Pfeifer, and U W Schnyder
[Gardner's syndrome].
August 1965, Schweizerische medizinische Wochenschrift,
W Fuhrmann, and K H Kärcher, and H Pfeifer, and U W Schnyder
Gardner's syndrome.
January 1973, Acta chirurgica Scandinavica,
W Fuhrmann, and K H Kärcher, and H Pfeifer, and U W Schnyder
Gardner's syndrome.
September 1975, Journal of oral surgery (American Dental Association : 1965),
W Fuhrmann, and K H Kärcher, and H Pfeifer, and U W Schnyder
Gardner's syndrome.
February 1966, The American journal of roentgenology, radium therapy, and nuclear medicine,
W Fuhrmann, and K H Kärcher, and H Pfeifer, and U W Schnyder
[Gardner's syndrome].
December 1994, Nihon rinsho. Japanese journal of clinical medicine,
Copied contents to your clipboard!