Results 1 to 10 of about 338 (94)

Retro- and orthonasal olfactory function in relation to olfactory bulb volume in patients with hypogonadotrophic hypogonadism [PDF]

Brazilian Journal of Otorhinolaryngology, 2018
Introduction: Idiopathic hypogonadotrophic hypogonadism with an olfactory deficit is defined as Kallmann syndrome and is distinct from normosmic idiopathic hypogonadotrophic hypogonadism.
Murat Salihoglu, Onuralp Kurt, Seyid Ahmet Ay, Kamil Baskoy, Aytug Altundag, Muzaffer Saglam, Ferhat Deniz, Hakan Tekeli, Arif Yonem, Thomas Hummel   +9 more
doaj   +2 more sources

Kallmann Syndrome. Case presentation [PDF]

Medisur, 2016
Kallmann syndrome is characterized by the association of hypogonadotropic hypogonadism and anosmia. It affects one of every 10 000 and 50 000 women.
Elodia Rivas Alpízar, Maidelín Garcés Saborit, Caridad Hernández Gutiérrez, Odalis Yanes Izray   +3 more
doaj   +4 more sources

Misceláneos [PDF]

Revista Colombiana de Endocrinología, Diabetes y Metabolismo, 2019
Listado: • Amenorrea primaria e hiposmia: diagnóstico tardío del síndrome de Kallmann en una mujer.   Ramírez A, Tutal L, Barakat S, Abreu A. • Análisis de la dinámica de las variables morfológicas y de actividad física en estudiantes de Medicina.
Asociación Colombiana de Endocrinología Diabetes y Metabolismo
doaj   +3 more sources

Diagnostic yield of clinical exome sequencing in congenital hypogonadotropic hypogonadism considering the degree of olfactory impairment

Anales de Pediatría (English Edition), 2022
Introduction: Congenital hypogonadotropic hypogonadism (CHH) can present alone or in association with anosmia or other congenital malformations. More than 30 genes have been identified as being involved in the pathogenesis of CHH with different patterns ...
Nelmar Valentina Ortiz-Cabrera, Teresa Gavela-Pérez, Francisco Javier Mejorado-Molano, Jessica Mire Santillán-Coello, José Miguel Villacampa-Aubá, María José Trujillo-Tiebas, Leandro Soriano-Guillén   +6 more
doaj   +1 more source

HIPOGONADISMO HIPOGONADOTRÓFICO COM DISFUNÇÃO ERÉTIL COMO MANIFESTAÇÃO DE HEMOCROMATOSE, UM RELATO DE CASO

Hematology, Transfusion and Cell Therapy, 2023
Introdução: A hemocromatose é uma patologia caracterizada por sobrecarga de ferro associada à eritropoiese normal, aumento da transferrina, ferro sérico e deposição parenquimatosa de ferro causada por baixos níveis de hepcidina.
LV Silva, MLRC Andrade, PA Silva, RIN Rocha, AM Vanderlei, LBC Fontes, MFH Costa, MCB Correia   +7 more
doaj   +1 more source

Wypieranie eponimów medycznych związanych z reżimem nazistowskim na przykładzie zmian w Międzynarodowej Klasyfikacji Chorób Światowej Organizacji Zdrowia [PDF]

, 2021
This work focuses on a specific type of terminological variants, i.e. medical eponymous terms gradually replaced by alternative, noneponymous terms.
Karwacka, Wioleta
core   +2 more sources

Análisis del rendimiento de la secuenciación del exoma clínico en hipogonadismo hipogonadotropo congénito teniendo en cuenta el grado de alteración del olfato. [PDF]

, 2021
Introduction: Congenital hypogonadotropic hypogonadism (CHH) can present alone or in association with anosmia or other congenital malformations. More than 30 genes have been identified as being involved in the pathogenesis of CHH with different patterns ...
Mejorado-Molano, Francisco Javier, Ortiz-Cabrera, Nelmar Valentina, Santillán-Coello, Jessica Mire, Soriano Guillén, Leandro, Trujillo-Tiebas, María José, Villacampa-Aubá, José Miguel   +5 more
core   +1 more source

Kallmann syndrome: a hystorical, clinical and molecular review [PDF]

, 2008
Kallmann syndrome (KS), the association of hypogonadotropic hypogonadism and anosmia, was described by Maestre de San Juan in 1856 and characterized as a hereditary condition by Franz Josef Kallmann in 1944.
Albuisson J, Bagatell CJ, Bardin CW, Bauman A, Bulow HE, Chryssikopoulos A, Davidson TM, De Morsier G, Dode C, Dode C, Dode C, Doty RL, Filippi G, Franco B, Fromantin M, Gonzalez-Martinez D, Gonzalez-Martinez D, Groth C, Hardelin JP, Hebert JM, Hipkin LJ, Julio Abucham, Kadva A, Kallmann FJ, Kramer PR, Legouis R, Li M, Lin DC, Maestre de San Juan A, Matsuo T, Mayston MJ, Meitinger T, Miura K, Muenke M, Muller-Hill B, Naftolin F, Okubo K, Oliveira LM, Parenti G, Pawlowitzki IH, Pitteloud N, Pitteloud N, Pitteloud N, Quinton R, Quinton R, Quinton R, Rezvani I, Ribeiro RS, Rogol AD, Rogério Silicani Ribeiro, Rowe RC, Rugarli EI, Sato N, Schwanzel-Fukuda M, Schwanzel-Fukuda M, Seminara SB, Simon MA, Soussi-Yanicostas N, Soussi-Yanicostas N, Trarbach EB, Trarbach EB, Vermeulen A, Waldstreicher J, Wray S   +63 more
core   +3 more sources

Amenorrea primaria

Revista Colombiana de Obstetricia y Ginecología, 2009
Objetivo: se hace una revisión detallada de la amenorreaprimaria, teniendo como base la clasificación propuesta por Mashchak CA y col. de acuerdo con la presencia o ausencia del desarrollo mamario y la presencia o no de útero, por ser la de mayor ...
Janer Sepúlveda-Agudelo, Miguel Ángel Alarcón-Nivia, Hermes Jaimes-Carvajal   +2 more
doaj   +1 more source

Rare causes of amenorrhea due to hypogonadotropic hypogonadism [PDF]

, 2023
El hipogonadismo hipogonadotrópico es un síndrome clínico de diversas etiologías congénitas o adquiridas, las cuales pueden o no causar amenorrea, ya sea primaria o secundaria, entre otros trastornos de la pubertad.
Castro Fernández, Melissa, Gamboa Miranda, Sofía, Guevara Sigarán, María Fernanda   +2 more
core   +2 more sources