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Pituitary|October 19, 2022
Idiopathic central diabetes insipidus in a large cohort of patients: the hypopituitarism ENEA rare observational (HEROS) studyH Masri Iraqi, E Pigarova, S Zacharieva, et al.
Medicina Clinica|July 11, 2006
[Usefulness of analysis of cerebrospinal fluid for the diagnosis of neurotransmitters and pterin defects and glucose and folate transport deficiencies across blood brain barrier]Aida Ormazabal, Angels García Cazorla, Belén Pérez Dueñas, et al.
Nature Genetics|October 5, 2001
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxinM C Moreira, C Barbot, N Tachi, et al.
The American Journal of Clinical Nutrition|February 8, 2013
Intestinal absorption rate in children after small intestinal transplantationFelipe Ordonez, Laurence Barbot-Trystram, Florence Lacaille, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 15, 2014
Intestinal deletion of leptin signaling alters activity of nutrient transporters and delayed the onset of obesity in miceAnnabelle Tavernier, Jean-Baptiste Cavin, Maude Le Gall, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|May 12, 2021
A High-Affinity Calmodulin-Binding Site in the CyaA Toxin Translocation Domain is Essential for Invasion of Eukaryotic CellsAlexis Voegele, Mirko Sadi, Darragh Patrick O'Brien, et al.
International Journal of Clinical Practice|April 29, 2021
Impact of a medication reconciliation care bundle at hospital discharge on continuity of care: A randomised controlled trialFrédérique Bouchand, Céline Leplay, Ricardo Guimaraes, et al.
European Journal of Endocrinology|December 20, 2023
A novel somatostatin receptor ligand for human ACTH - and GH -secreting pituitary adenomasDaniela Regazzo, Serena Avallone, Cliona P MacSweeney, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 3, 2008
Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation typeTeresa Temudo, Elisabete Ramos, Karin Dias, et al.
Orphanet Journal of Rare Diseases|July 27, 2016
Increased red cell distribution width in Fanconi anemia: a novel marker of stress erythropoiesisRosa Sousa, Cristina Gonçalves, Isabel Couto Guerra, et al.
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