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Péter Gergics

Showing results (1-10 of 10) with videos related to

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Orvosi Hetilap|February 13, 2018
[Genetic factors in hypopituitarism. The role of transcription factors in pituitary hormone deficiency]Judit Tőke, Rita Bertalan, Péter Gergics, et al.
European Journal of Pediatrics|June 20, 2007
Orolabial signs are important clues for diagnosis of the rare endocrine syndrome MEN 2B. Presentation of two unrelated casesAgnes Sallai, Eva Hosszú, Péter Gergics, et al.
Wiener Klinische Wochenschrift|June 30, 2009
Parathyroid hormone-dependent hypercalcemiaJudit Toke, Attila Patócs, Katalin Balogh, et al.
Orvosi Hetilap|April 14, 2009
[Extracellular calcium sensing under normal and pathological conditions]Judit Toke, Attila Patócs, Péter Gergics, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|July 16, 2005
Rapid re-enlargement of a macroprolactinoma after initial shrinkage in a young woman treated with bromocriptineIldikó Adler, Péter Barsi, Sándor Czirják, et al.
Clinical Endocrinology|June 9, 2007
Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium-sensing receptor geneJudit Tõke, Gábor Czirják, Attila Patócs, et al.
The Journal of Steroid Biochemistry and Molecular Biology|November 30, 2010
The 83,557insA variant of the gene coding 11β-hydroxysteroid dehydrogenase type 1 enzyme associates with serum osteocalcin in patients with endogenous Cushing's syndromeAgnes Szappanos, Attila Patócs, Péter Gergics, et al.
Orvosi Hetilap|December 3, 2009
[Methods for the analysis of large gene deletions and their application in some hereditary diseases]Péter Gergics, Judit Toke, Agnes Szilágyi, et al.
Orvosi Hetilap|December 6, 2005
[Clinical symptoms, diagnosis and treatment of multiple endocrine neoplasia type 1. Results of genetic screening in Hungarian patients]Katalin Balogh, László Hunyady, Attila Patócs, et al.
Orvosi Hetilap|January 11, 2007
[Nucleotide sequence variants of the glucocorticoid receptor gene and their significance in determining glucocorticoid sensitivity]Judit Majnik, Attila Patócs, Katalin Balogh, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Orvosi Hetilap|February 13, 2018
[Genetic factors in hypopituitarism. The role of transcription factors in pituitary hormone deficiency]Judit Tőke, Rita Bertalan, Péter Gergics, et al.
European Journal of Pediatrics|June 20, 2007
Orolabial signs are important clues for diagnosis of the rare endocrine syndrome MEN 2B. Presentation of two unrelated casesAgnes Sallai, Eva Hosszú, Péter Gergics, et al.
Wiener Klinische Wochenschrift|June 30, 2009
Parathyroid hormone-dependent hypercalcemiaJudit Toke, Attila Patócs, Katalin Balogh, et al.
Orvosi Hetilap|April 14, 2009
[Extracellular calcium sensing under normal and pathological conditions]Judit Toke, Attila Patócs, Péter Gergics, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|July 16, 2005
Rapid re-enlargement of a macroprolactinoma after initial shrinkage in a young woman treated with bromocriptineIldikó Adler, Péter Barsi, Sándor Czirják, et al.
Clinical Endocrinology|June 9, 2007
Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium-sensing receptor geneJudit Tõke, Gábor Czirják, Attila Patócs, et al.
The Journal of Steroid Biochemistry and Molecular Biology|November 30, 2010
The 83,557insA variant of the gene coding 11β-hydroxysteroid dehydrogenase type 1 enzyme associates with serum osteocalcin in patients with endogenous Cushing's syndromeAgnes Szappanos, Attila Patócs, Péter Gergics, et al.
Orvosi Hetilap|December 3, 2009
[Methods for the analysis of large gene deletions and their application in some hereditary diseases]Péter Gergics, Judit Toke, Agnes Szilágyi, et al.
Orvosi Hetilap|December 6, 2005
[Clinical symptoms, diagnosis and treatment of multiple endocrine neoplasia type 1. Results of genetic screening in Hungarian patients]Katalin Balogh, László Hunyady, Attila Patócs, et al.
Orvosi Hetilap|January 11, 2007
[Nucleotide sequence variants of the glucocorticoid receptor gene and their significance in determining glucocorticoid sensitivity]Judit Majnik, Attila Patócs, Katalin Balogh, et al.
Pageof 1