Results 121 to 130 of about 2,220 (203)

Forty years of the adrenal chromaffin cell through ISCCB meetings around the world. [PDF]

Pflugers Arch, 2023
Maneu V, Borges R, Gandía L, García AG.   +3 more
europepmc   +1 more source

Case Report: Late diagnosis of McCune-Albright with severe kyphoscoliosis, acromegaly and tertiary hyperparathyroidism. [PDF]

Front Endocrinol (Lausanne)
Bogusławska A, Komisarz-Calik M, Hubalewska-Dydejczyk A, Korbonits M, Romanet P, Barlier A, Gilis-Januszewska A.   +6 more
europepmc   +1 more source

Age-independent anti-angiogenic therapy for choroidal neovascularization by targeting secretogranin III. [PDF]

Geroscience
Huang C, Tian H, Li W.
europepmc   +1 more source

Bronchial salivary gland-type mucinous adenocarcinoma harboring a GNAS mutation: a novel lung cancer entity? A case report. [PDF]

Virchows Arch
Chen C, Wu H, Yin W, Shi X, Zhao Y.
europepmc   +1 more source

Neuroendocrine Cells in Barrett's Mucosa and Adenocarcinomas of the Gastroesophageal Junction [PDF]

, 2004
Dekken, H. (Herman) van, Dinjens, W.N.M. (Winand), Koppert, L.B. (Linetta), Stijnen, Th. (Theo), Tilanus, H.W. (Hugo), Wijnhoven, B.P.L. (Bas)   +5 more
core   +3 more sources

Peripheral catecholamine systems: an evolutionary perspective. [PDF]

Am J Physiol Regul Integr Comp Physiol
Goldstein DS.
europepmc   +1 more source

Bronchial Carcinoid as a Cause of Hemoptysis [PDF]

, 2013
Akidiva, Samuel, Bhanot, Deepa, Hagan, Stephen F   +2 more
core   +2 more sources

Early Manifestation of McCune-Albright Syndrome in a 32-Month-Old Female: A Rare Case Report. [PDF]

J Investig Med High Impact Case Rep
Makhlouf TZ, Mahareeq MS, Abumazen A, Manasrah T, Badareen M, Zighan MS.   +5 more
europepmc   +1 more source

Quantifying Intracellular Single Vesicular Catecholamine Concentration with Open Carbon Nanopipettes to Unveil the Effect of L-DOPA on Vesicular Structure. [PDF]

Angew Chem Int Ed Engl, 2022
Hu K, Le Vo KL, Hatamie A, Ewing AG.
europepmc   +1 more source

Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations. [PDF]

Mov Disord Clin Pract
Magistrelli L, Contaldi E, Piola B, Caushi F, Carecchio M, D'Alfonso S, Corrado L.   +6 more
europepmc   +1 more source