BIOMAT Database Logo BIOMAT Database Logo

[Hypothalamo-hypophyseal dwarfism with spontaneous puberty]. 1961

J M ANTONIN

UI MeSH Term Description Entries
D008499 Medical Records Recording of pertinent information concerning patient's illness or illnesses. Health Diaries,Medical Transcription,Records, Medical,Transcription, Medical,Diaries, Health,Diary, Health,Health Diary,Medical Record,Medical Transcriptions,Record, Medical,Transcriptions, Medical
D011627 Puberty A period in the human life in which the development of the hypothalamic-pituitary-gonadal system takes place and reaches full maturity. The onset of synchronized endocrine events in puberty lead to the capacity for reproduction (FERTILITY), development of secondary SEX CHARACTERISTICS, and other changes seen in ADOLESCENT DEVELOPMENT. Puberties
D004392 Dwarfism A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height. Nanism
D004393 Dwarfism, Pituitary A form of dwarfism caused by complete or partial GROWTH HORMONE deficiency, resulting from either the lack of GROWTH HORMONE-RELEASING FACTOR from the HYPOTHALAMUS or from the mutations in the growth hormone gene (GH1) in the PITUITARY GLAND. It is also known as Type I pituitary dwarfism. Human hypophysial dwarf is caused by a deficiency of HUMAN GROWTH HORMONE during development. Growth Hormone Deficiency Dwarfism,Hypophysial Dwarf,Hyposomatotrophic Dwarfism,Pituitary Dwarf,Dwarfism, Growth Hormone Deficiency,Isolated GH Deficiency,Isolated Growth Hormone Deficiency,Isolated HGH Deficiency,Isolated Human Growth Hormone Deficiency,Isolated Somatotropin Deficiency,Isolated Somatotropin Deficiency Disorder,Nanism, Pituitary,Pituitary Dwarfism,Pituitary Nanism
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D012741 Sexual Maturation Achievement of full sexual capacity in animals and in humans. Sex Maturation,Maturation, Sex,Maturation, Sexual

Related Publications

J M ANTONIN
[Endocrine dwarfism. 2. Treatment of hypothalamo-hypophyseal dwarfism and of constitutional dwarfism with postponement of puberty].
April 1975, Kinderarztliche Praxis,
J M ANTONIN
[Endocrine dwarfism. I. Diagnosis and differential diagnosis of hypothalamo-hypophyseal dwarfism].
February 1975, Kinderarztliche Praxis,
J M ANTONIN
[Hypothalamo-hypophyseal dwarfism with inner ear deafness in 2 sisters].
February 1972, Der Internist,
J M ANTONIN
[Hypothalamo-hypophyseal maturation of puberty. Experimental data].
December 1982, Annales d'endocrinologie,
J M ANTONIN
Hereditary pituitary dwarfism with spontaneous puberty.
February 1968, Archives of disease in childhood,
J M ANTONIN
Hypothalamo-hypophyseal-gonadal function in boys with irregular puberty.
January 1983, Neuroscience and behavioral physiology,
J M ANTONIN
[Genetic basis of familial multihormonal hypothalamo-hypophyseal dwarfism in children].
January 1977, Endokrynologia Polska,
J M ANTONIN
[Growth hormone of human origin and treatment of hypothalamo-hypophyseal dwarfism].
February 1966, Bruxelles medical,
J M ANTONIN
[Genetic basis of the familial form of hypothalamo-hypophyseal dwarfism in children].
October 1978, Ceskoslovenska pediatrie,
J M ANTONIN
[Growth hormone deficiency dwarfism and idiopathic hypopituitarism. Study of hypothalamo-hypophyseal function].
July 1973, Revista clinica espanola,
Copied contents to your clipboard!