Zobrazeno 1 - 10 of 12 pro vyhledávání: '"S. A. Seminara"'
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Akademický článek
Anomalous Diffusion with Caputo-Fabrizio Time Derivative: an Inverse Problem.
Autor: S. A. Seminara, M. I. Troparevsky, M. A. Fabio, G. La Mura
Publikováno v: Trends in Computational and Applied Mathematics, Vol 23, Iss 3 (2022)
In this work we approximate the source for a non homogeneous fractional diffusion equation in 1D, from measurements of the concentration at a finite number of points. We use Caputo-Fabrizio time fractional derivative to model anomalous diffusion. Sep
Externí odkaz: https://doaj.org/article/0a28d6303c1f4aebb471a3d403724d97
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3
HYPOGONADOTROPIC HYPOGONADISM
Autor: F J, Hayes, S B, Seminara, W F, Crowley
Publikováno v: Endocrinology and Metabolism Clinics of North America. 27:739-763
This article outlines the changing pattern of gonadotropin-releasing hormone (GnRH)-induced gonadotropin secretion across sexual development, a knowledge of which is critical to understanding GnRH secretion in pathologic states such as hypogonadotrop
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3583f2b5b3ea0c14bf85a496d7c6192a
https://doi.org/10.1016/s0889-8529(05)70039-6
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6
The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics
Autor: L M, Oliveira, S B, Seminara, M, Beranova, F J, Hayes, S B, Valkenburgh, E, Schipani, E M, Costa, A C, Latronico, W F, Crowley, M, Vallejo
Publikováno v: The Journal of clinical endocrinology and metabolism. 86(4)
Kallmann syndrome (KS) consists of congenital, isolated, idiopathic hypogonadotropic hypogonadism (IHH) and anosmia. The gene responsible for the X-linked form of KS, KAL, encodes a protein, anosmin, that plays a key role in the migration of GnRH neu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::138eaa04d7430b138ab2cde233ec73ec
https://pubmed.ncbi.nlm.nih.gov/11297579
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7
Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism
Autor: M, Beranova, L M, Oliveira, G Y, Bédécarrats, E, Schipani, M, Vallejo, A C, Ammini, J B, Quintos, J E, Hall, K A, Martin, F J, Hayes, N, Pitteloud, U B, Kaiser, W F, Crowley, S B, Seminara
Publikováno v: The Journal of clinical endocrinology and metabolism. 86(4)
Mutations in the GnRH receptor (GNRHR) have been described as a cause of reproductive failure in a subset of patients with idiopathic hypogonadotropic hypogonadism (IHH). Given the apparent rarity of these mutations, we set out to determine the frequ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0bc69c2ccf58224fad2848977e1bba02
https://pubmed.ncbi.nlm.nih.gov/11297587
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8
Differential regulation of gonadotropin secretion by testosterone in the human male: absence of a negative feedback effect of testosterone on follicle-stimulating hormone secretion
Autor: F J, Hayes, S, DeCruz, S B, Seminara, P A, Boepple, W F, Crowley
Publikováno v: The Journal of clinical endocrinology and metabolism. 86(1)
Studies of sex steroid regulation of gonadotropin secretion in the human male have focused primarily on the respective site(s) of negative feedback of testosterone (T) and estradiol (E(2)). The use of pharmacological doses of sex steroids in these st
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7684718e84166e8aaa2eb9cc7605da40
https://pubmed.ncbi.nlm.nih.gov/11231978
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9
Successful use of pulsatile gonadotropin-releasing hormone (GnRH) for ovulation induction and pregnancy in a patient with GnRH receptor mutations
Autor: S B, Seminara, M, Beranova, L M, Oliveira, K A, Martin, W F, Crowley, J E, Hall
Publikováno v: The Journal of clinical endocrinology and metabolism. 85(2)
GnRH receptor mutations have recently been identified in a small number of familial cases of nonanosmic hypogonadotropic hypogonadism. In the present report we studied a kindred in which two sisters with primary amenorrhea were affected with GnRH def
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::952810a883d19a892dea132f0566429e
https://pubmed.ncbi.nlm.nih.gov/10690855
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10
X-linked adrenal hypoplasia congenita: a mutation in DAX1 expands the phenotypic spectrum in males and females
Autor: S B, Seminara, J C, Achermann, M, Genel, J L, Jameson, W F, Crowley
Publikováno v: The Journal of clinical endocrinology and metabolism. 84(12)
X-linked adrenal hypoplasia congenita (AHC) is a disorder associated with primary adrenal insufficiency and hypogonadotropic hypogonadism (HH). The gene responsible for X-linked AHC, DAX1, encodes a member of the nuclear hormone receptor superfamily.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::330c0e3a14a59a65c7ae6e08e2ac18da
https://pubmed.ncbi.nlm.nih.gov/10599709
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