Results 131 to 140 of about 6,751 (239)

Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis [PDF]

open access: yes, 2017
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]

open access: bronze, 2006
Ofer Arnon   +5 more
openalex   +1 more source

Stinging Nettle (Urtica dioica): An Unusual Case of Galactorrhea

open access: hybrid, 2021
Laura Easton   +4 more
openalex   +1 more source

Galactorrhea in infant induced by maternal antidepressants use: case report

open access: diamond, 2023
Érica Batalha Gomes   +6 more
openalex   +2 more sources

A Case of Paroxetine-Induced Galactorrhea [PDF]

open access: bronze, 2002
Eric Davenport, Raj Velamoor
openalex   +1 more source

Management for prolactinomas of postmenopausal female patients: a retrospective single-center study. [PDF]

open access: yesBMC Endocr Disord
Chen X   +10 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy