Page last updated: 2024-08-17

levodopa and Cretinism

levodopa has been researched along with Cretinism in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (33.33)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (33.33)	29.6817
2010's	1 (33.33)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Álvarez-Sabin, J; Boronat-Guerrero, S; Hernández-Vara, J; Salvado, M	1
Asmus, F; Gasser, T; Horber, V; Munz, M; Pohlenz, J; Schöning, M; Schwabe, D; Zimprich, A	1
Asfour, M; Fossati, P; Foulinnie, JC; Golstein, J; Granier, F; L'Hermite, M; Lefèbvre, J	1

Reviews

1 review(s) available for levodopa and Cretinism

Article	Year
[Chorea due to TITF1/NKX2-1 mutation: phenotypical description and therapeutic response in a family]. Revista de neurologia, 2013, May-16, Volume: 56, Issue:10 Topics: Adolescent; Adult; Age of Onset; Brain; Carbidopa; Chorea; Congenital Hypothyroidism; Drug Therapy, Combination; Exons; Female; Humans; Infant, Newborn; Intellectual Disability; Levodopa; Magnetic Resonance Imaging; Nuclear Proteins; Pedigree; Phenotype; Pregnancy; Sequence Deletion; Thyroid Nuclear Factor 1; Transcription Factors; Young Adult	2013

Article

Year

[Chorea due to TITF1/NKX2-1 mutation: phenotypical description and therapeutic response in a family].

Revista de neurologia, 2013, May-16, Volume: 56, Issue:10

Topics: Adolescent; Adult; Age of Onset; Brain; Carbidopa; Chorea; Congenital Hypothyroidism; Drug Therapy, Combination; Exons; Female; Humans; Infant, Newborn; Intellectual Disability; Levodopa; Magnetic Resonance Imaging; Nuclear Proteins; Pedigree; Phenotype; Pregnancy; Sequence Deletion; Thyroid Nuclear Factor 1; Transcription Factors; Young Adult

2013

Other Studies

2 other study(ies) available for levodopa and Cretinism

Article	Year
A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa. Neurology, 2005, Jun-14, Volume: 64, Issue:11 Topics: Child; Child, Preschool; Chorea; Codon, Nonsense; Congenital Hypothyroidism; DNA Mutational Analysis; Dopamine Agents; Exons; Fatal Outcome; Female; Genetic Testing; Humans; Levodopa; Male; Nuclear Proteins; Pedigree; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Thyroid Nuclear Factor 1; Transcription Factors; Treatment Outcome	2005
[The sella turcica and pituitary function in congenital hypothyroidism due to thyroid ectopia or hypogenesis (author's transl)]. La Nouvelle presse medicale, 1977, Dec-31, Volume: 6, Issue:45 Topics: Adolescent; Adult; Arginine; Circadian Rhythm; Congenital Hypothyroidism; Female; Growth Hormone; Humans; Hypothyroidism; Insulin; Levodopa; Male; Middle Aged; Pituitary Function Tests; Pituitary Gland; Prolactin; Radiography; Sella Turcica; Thyroid Gland; Thyrotropin; Thyrotropin-Releasing Hormone	1977

Article

Year

A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa.

Neurology, 2005, Jun-14, Volume: 64, Issue:11

Topics: Child; Child, Preschool; Chorea; Codon, Nonsense; Congenital Hypothyroidism; DNA Mutational Analysis; Dopamine Agents; Exons; Fatal Outcome; Female; Genetic Testing; Humans; Levodopa; Male; Nuclear Proteins; Pedigree; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Thyroid Nuclear Factor 1; Transcription Factors; Treatment Outcome

2005

[The sella turcica and pituitary function in congenital hypothyroidism due to thyroid ectopia or hypogenesis (author's transl)].

La Nouvelle presse medicale, 1977, Dec-31, Volume: 6, Issue:45

Topics: Adolescent; Adult; Arginine; Circadian Rhythm; Congenital Hypothyroidism; Female; Growth Hormone; Humans; Hypothyroidism; Insulin; Levodopa; Male; Middle Aged; Pituitary Function Tests; Pituitary Gland; Prolactin; Radiography; Sella Turcica; Thyroid Gland; Thyrotropin; Thyrotropin-Releasing Hormone

1977