Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Salvatore Scommegna"'
Autor:
Andrea Zangari, Carmine Noviello, Camilla Todesco, Mercedes Romano, Letizia Trotta, Carmine Botta, Ilaria Cascone, Salvatore Scommegna, Gabriele Vasta, Vito Briganti, Alfonso Papparella
Publikováno v:
La Pediatria Medica e Chirurgica, Vol 46, Iss 2 (2024)
Gynecomastia is a benign glandular proliferation that can affect adolescents causing significant psychological discomfort. Generally, it is idiopathic but underlying endocrinological conditions must be excluded. Different surgical techniques are avai
Externí odkaz:
https://doaj.org/article/f841e724230345bd8c4e52b9cc0811ec
Autor:
Giovanni Neri, Salvatore Scommegna, Brunetto Boscherini, Daniela Orteschi, Daniela Galeazzi, Emanuela Lucci-Cordisco
Publikováno v:
American Journal of Medical Genetics Part A. :2750-2755
Anterior pituitary aplasia (APA) is a very rare cause of congenital-onset multiple pituitary hormone deficiency (CO-MPHD). We report on molecular analysis and clinical follow-up of three previously reported cases of APA [Scommegna et al., 2004], who
Autor:
Francesca Mazzoli, Alison Shardlow, Matteo Chinello, Cinzia Ciccacci, Salvatore Scommegna, Anna Locasciulli, Nadia De Giovanni, Nadia Fucci, Mauro Calvani, Paola Borgiani
Publikováno v:
Pediatric Emergency Care. 33:344-345
We report a case of mild cannabinoid poisoning in a preschool child, after 3-week ingestion of hemp seed oil prescribed by his pediatrician to strengthen his immune system. The patient presented neurological symptoms that disappeared after intravenou
Autor:
Rocco Agostino, Edoardo Farinelli, Simonetta Picone, Brunetto Boscherini, Salvatore Scommegna, Stefano Cianfarani, Daniela Galeazzi, Alessandro Bozzao
Publikováno v:
Hormone Research in Paediatrics. 62:10-16
Background: Neonatal onset hypopituitarism is a life-threatening, potentially treatable endocrine disease. A possible cause is congenital absence of the anterior pituitary gland, a condition very rarely reported in the literature. Methods: A series o
Autor:
Carmelilia De Bernardo, Giacinto Marrocco, Anna Maria Rapone, Luigi Laino, Irene Bottillo, Silvia Majore, Barbara Grammatico, Salvatore Scommegna, Paola Grammatico, Nicoletta Preziosi
Publikováno v:
Endocrine Connections
Sex development is a process under genetic control directing both the bi-potential gonads to become either a testis or an ovary, and the consequent differentiation of internal ducts and external genitalia. This complex series of events can be altered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a772596f81e6ab2bf11de6969589f729
http://hdl.handle.net/11573/617465
http://hdl.handle.net/11573/617465
Autor:
Paola Grammatico, Lucia Pedace, Maria Stella Valentini, Nino Guarino, Brunetto Boscherini, Carmelilia De Bernardo, Giacinto Marrocco, Salvatore Scommegna, Anna Maria Rapone, Nicoletta Preziosi, Luigi Laino, Silvia Majore
Publikováno v:
American journal of medical genetics. Part A. (11)
Steroidogenic factor 1 (encoded by the NR5A1 gene) is a critical regulator of reproduction, controlling transcription of key genes involved in sexual dimorphism. To date, NR5A1 variants have been found in individuals with a 46,XY karyotype and gonada
Autor:
Silvia Majore, Salvatore Scommegna, Paola Grammatico, Anna Maria Rapone, Luciana Ungaro, Aldo Morrone, Nino Guarino, Giacinto Marrocco
Publikováno v:
Frontiers in Endocrinology, Vol 4 (2013)
Frontiers in Endocrinology
Frontiers in Endocrinology
One of the most common problem found in patients with Disorders of Sexual Developments is the absence or extreme hypoplasia of the vagina. The type of patients presenting this anomaly may belong to completely different groups: (1) Patients with a uro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bbaf1716563f5c4f04bee4e891187fc
http://hdl.handle.net/11573/524209
http://hdl.handle.net/11573/524209
Autor:
Francesco Binni, Marco Castori, Alberto Pingi, Lucia Pedace, Salvatore Scommegna, Silvia Majore, Barbara Grammatico, Paola Grammatico
Anophthalmia/microphthalmia is a rare developmental craniofacial defect, which recognizes a wide range of causes, including chromosomal abnormalities, single-gene mutations as well as environmental factors. Heterozygous mutations in the SOX2 gene are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5f042014749da7b8ddc11d092ee9715
http://hdl.handle.net/11573/117580
http://hdl.handle.net/11573/117580
Autor:
Salvatore, Scommegna, Daniela, Galeazzi, Simonetta, Picone, Edoardo, Farinelli, Rocco, Agostino, Alessandro, Bozzao, Brunetto, Boscherini, Stefano, Cianfarani
Publikováno v:
Hormone research. 62(1)
Neonatal onset hypopituitarism is a life-threatening, potentially treatable endocrine disease. A possible cause is congenital absence of the anterior pituitary gland, a condition very rarely reported in the literature.A series of 5 cases of children