Results 101 to 110 of about 3,243 (180)

Spectral signatures of mirror movements in the sensori‐motor connectivity in kallmann syndrome [PDF]

, 2017
Renzo Manara, Federica Di Nardo, Alessandro Salvalaggio, Antonio Agostino Sinisi, G. Bonanni, Vincenzo Davide Palumbo, Elena Cantone, Arturo Brunetti, Francesco Di Salle, Arianna D'Errico, Andrea Elefante, Fabrizio Esposito   +11 more
openalex   +1 more source

A novel missense variant of FGFR1 in a Japanese girl with Kallmann syndrome and holoprosencephaly. [PDF]

Clin Pediatr Endocrinol, 2023
Uchida N, Mizuno Y, Seno S, Koyama Y, Takahashi T, Shibata H, Narumi S, Hasegawa T, Ishii T.   +8 more
europepmc   +1 more source

Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients [PDF]

, 2013
Julie Sarfati, Corinne Fouveaut, Chrystel Leroy, Marc Jeanpierre, Jean‐Pierre Hardelin, Catherine Dodé   +5 more
openalex   +1 more source

Mutation spectrum of Kallmann syndrome: identification of five novel mutations across ANOS1 and FGFR1. [PDF]

Reprod Biol Endocrinol, 2023
Chu G, Li P, Zhao Q, He R, Zhao Y.
europepmc   +1 more source

Identification and Functional Characterization of a Novel Variant in the SEMA3A Gene in a Chinese Family with Kallmann Syndrome. [PDF]

Int J Endocrinol, 2022
Shu M, Wu H, Wei S, Shi Y, Li Z, Cheng Y, Fang L, Xu C.   +7 more
europepmc   +1 more source

Diagnosis and therapy of Kallmann syndrome in a boy (real case)

, 2013
O. A. Oganova
openalex   +2 more sources

Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome [PDF]

, 2008
Ana Paula Abreu, Ericka Barbosa Trarbach, Margaret de Castro, Elaine Maria Frade Costa, Beatriz R. Versiani, Maria Tereza Matias Baptista, Heraldo Mendes Garmes, Berenice B. Mendonça, Ana Cláudia Latronico   +8 more
openalex   +1 more source

Kallmann syndrome and idiopathic hypogonadotropic hypogonadism: The role of semaphorin signaling on GnRH neurons

, 2021
Anna Cariboni, Ravikumar Balasubramanian
openalex   +2 more sources

Mirror Movements and Ichthyosis in a Child: A Rare Presentation of Kallmann Syndrome. [PDF]

Ann Indian Acad Neurol
Vachher H, Gandhi D, Pachapure S, Kamate M.   +3 more
europepmc   +1 more source

Convergent biological pathways underlying the Kallmann syndrome-linked genes Hs6st1 and Fgfr1. [PDF]

Hum Mol Genet, 2022
Moon S, Zhao YT.
europepmc   +1 more source