L. Persani

Type de document

Co-auteur

N. Pitteloud

M. Bonomi

J. Young

C. Xu

V. Vezzoli

A. Troendle

M.A. Stefanija

N. Smith

N. Skordis

N. Sato

R. Quinton

V. Popovic

D. Pignatelli

F. Phan-Hug

G.E. Papadakis

M. Niedziela

V. Neocleous

A. Morelli

F. Marelli

M.C. Lemos

B. Lecumberri

M. Lang-Muritano

P. Kumanov

S.-H. Kim

A. Juul

E. Hrabovszky

E. Hershkovitz

M. Hauschild

G. Guarnieri

P. Giacobini

C. Ghervan

A. A. Dwyer

P. Duminuco

S.P. Djurdjevic

W.S. Dhillo

M. Craen

L. Cotellessa

M. Cools

I. Borshchevsky

L. Bartoloni

C. Badiu

M. Adamo

Date

Source

Serveur académique Lausannois (2)

Mot-clé

Human beings (2) Hypogonadism (2) Evidence (2) puits (1) vertébré (1) enquête (1) statistiques (1) espèce (1) itinéraire (1) protéine (1) produit (1) information (1) analyse (1) santé (1) génétique (1) évaluation (1) maladie (1) âge (1) Nursing (1) Development (1) Defects (1) Care (1) Genetics (1) Platforms (1) Translations (1) Platforms (1) Drama (1) Translations (1) Identification (1) Statistics (1)

Documents écrit par L. Persani (2) | parle de L. Persani (0)

Defective jagged-1 signaling affects GnRH development and contributes to congenital hypogonadotropic hypogonadism.

L. Cotellessa et al. (8 mars 2023)

Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism.

C. Badiu et al. (20 mars 2017)