Results 131 to 140 of about 6,751 (239)
Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis [PDF]
Tyrosine hydroxylase deficiency is an autosomal recessive disorder resulting from cerebral catecholamine deficiency. Tyrosine hydroxylase deficiency has been reported in fewer than 40 patients worldwide. To recapitulate all available evidence on clinical
Aeby, Alec +31 more
core
Galactorrhea complicating wound healing following reduction mammaplasty [PDF]
Ofer Arnon +5 more
openalex +1 more source
Stinging Nettle (Urtica dioica): An Unusual Case of Galactorrhea
Laura Easton +4 more
openalex +1 more source
Galactorrhea in infant induced by maternal antidepressants use: case report
Érica Batalha Gomes +6 more
openalex +2 more sources
A Case of Paroxetine-Induced Galactorrhea [PDF]
Eric Davenport, Raj Velamoor
openalex +1 more source
Management for prolactinomas of postmenopausal female patients: a retrospective single-center study. [PDF]
Chen X +10 more
europepmc +1 more source
Evaluation of safety and efficacy of the combination of mebeverine and sulpiride in treatment of patients with functional gastrointestinal disorders: A prospective cohort. [PDF]
El-Kassas M +5 more
europepmc +1 more source

