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Albert Beckers

Showing results (101-110 of 175) with videos related to

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Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|June 11, 2020
Pancreatic Neuroendocrine Neoplasm Associated with a Familial MAX DeletionSandrine Petignot, Adrian F Daly, Emilie Castermans, et al.
Annales D'Endocrinologie|October 8, 2021
Thyroid cancer in the Democratic Republic of the Congo: Frequency and risk factorsJohn Bukasa Kakamba, Nadia Sabbah, Pascal Bayauli, et al.
Pituitary|June 12, 2016
Combined treatment with octreotide LAR and pegvisomant in patients with pituitary gigantism: clinical evaluation and genetic screeningRuth Mangupli, Liliya Rostomyan, Emilie Castermans, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|February 23, 2011
Aggressive prolactinoma in a child related to germline mutation in the ARYL hydrocarbon receptor interacting protein (AIP) geneLuciana Ansaneli Naves, Marie-Lise Jaffrain-Rea, Sergio Alberto Cunha Vêncio, et al.
European Journal of Endocrinology|August 18, 2009
Aggressive pituitary adenomas occurring in young patients in a large Polynesian kindred with a germline R271W mutation in the AIP geneJuliet E Jennings, Marianthi Georgitsi, Ian Holdaway, et al.
Endocrine-Related Cancer|January 5, 2017
Paleogenetic study of ancient DNA suggestive of X-linked acrogigantismAlbert Beckers, Daniel Fernandes, Frederic Fina, et al.
European Journal of Endocrinology|March 22, 2015
A novel inactivating mutation of the LH/chorionic gonadotrophin receptor with impaired membrane trafficking leading to Leydig cell hypoplasia type 1Adolfo Rivero-Müller, Iulia Potorac, Axelle Pintiaux, et al.
European Journal of Endocrinology|June 6, 2019
Compound heterozygous mutations in the luteinizing hormone receptor signal peptide causing 46,XY disorder of sex developmentIulia Potorac, Ashutosh Trehan, Kamila Szymańska, et al.
Familial Cancer|February 14, 2014
Deletion of exons 1-3 of the MEN1 gene in a large Italian family causes the loss of menin expressionMaria Chiara Zatelli, Federico Tagliati, Mauro Di Ruvo, et al.
The Journal of Clinical Endocrinology and Metabolism|June 4, 2010
The ratio of parathyroid hormone as measured by third- and second-generation assays as a marker for parathyroid carcinomaEtienne Cavalier, Adrian F Daly, Daniela Betea, et al.
Pageof 18

Showing results (101-110 of 175) with videos related to

Sort By:
Pageof 18
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|June 11, 2020
Pancreatic Neuroendocrine Neoplasm Associated with a Familial MAX DeletionSandrine Petignot, Adrian F Daly, Emilie Castermans, et al.
Annales D'Endocrinologie|October 8, 2021
Thyroid cancer in the Democratic Republic of the Congo: Frequency and risk factorsJohn Bukasa Kakamba, Nadia Sabbah, Pascal Bayauli, et al.
Pituitary|June 12, 2016
Combined treatment with octreotide LAR and pegvisomant in patients with pituitary gigantism: clinical evaluation and genetic screeningRuth Mangupli, Liliya Rostomyan, Emilie Castermans, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|February 23, 2011
Aggressive prolactinoma in a child related to germline mutation in the ARYL hydrocarbon receptor interacting protein (AIP) geneLuciana Ansaneli Naves, Marie-Lise Jaffrain-Rea, Sergio Alberto Cunha Vêncio, et al.
European Journal of Endocrinology|August 18, 2009
Aggressive pituitary adenomas occurring in young patients in a large Polynesian kindred with a germline R271W mutation in the AIP geneJuliet E Jennings, Marianthi Georgitsi, Ian Holdaway, et al.
Endocrine-Related Cancer|January 5, 2017
Paleogenetic study of ancient DNA suggestive of X-linked acrogigantismAlbert Beckers, Daniel Fernandes, Frederic Fina, et al.
European Journal of Endocrinology|March 22, 2015
A novel inactivating mutation of the LH/chorionic gonadotrophin receptor with impaired membrane trafficking leading to Leydig cell hypoplasia type 1Adolfo Rivero-Müller, Iulia Potorac, Axelle Pintiaux, et al.
European Journal of Endocrinology|June 6, 2019
Compound heterozygous mutations in the luteinizing hormone receptor signal peptide causing 46,XY disorder of sex developmentIulia Potorac, Ashutosh Trehan, Kamila Szymańska, et al.
Familial Cancer|February 14, 2014
Deletion of exons 1-3 of the MEN1 gene in a large Italian family causes the loss of menin expressionMaria Chiara Zatelli, Federico Tagliati, Mauro Di Ruvo, et al.
The Journal of Clinical Endocrinology and Metabolism|June 4, 2010
The ratio of parathyroid hormone as measured by third- and second-generation assays as a marker for parathyroid carcinomaEtienne Cavalier, Adrian F Daly, Daniela Betea, et al.
Pageof 18