Zobrazeno 1 - 10
of 307
pro vyhledávání: '"Segmental neurofibromatosis"'
Autor:
Hisato Iriki, MD, PhD, Noriko Umegaki-Arao, MD, PhD, Risa Kakuta, MD, PhD, Harumi Fujita, PhD, Satomi Aoki, Masayuki Amagai, MD, PhD, Takashi Sasaki, PhD, Yasuo Hamamoto, MD, PhD, Robert Nakayama, MD, PhD, Akiharu Kubo, MD, PhD
Publikováno v:
JAAD Case Reports, Vol 25, Iss , Pp 89-92 (2022)
Externí odkaz:
https://doaj.org/article/6545edb8676945d5a3359f55b8767f6e
Autor:
D. A. Gulyaev, I. Yu. Belov, D. V. Nizolin, L. B. Mitrofanova, N. A. Primak, D. S. Godanyuk, I. A. Kurnosov
Publikováno v:
Сибирский онкологический журнал, Vol 20, Iss 6, Pp 158-163 (2022)
Background. Neurofibromatosis is a fairly rare disease (1/3000). In 1992, V. Riccardi described seven types of neurofibromatosis. Segmental neurofibromatosis (sh), also known as type V neurofibromatosis, is an extremely rare variant characterized by
Externí odkaz:
https://doaj.org/article/e17fdaa99a834e289f9c41619dc9805f
Publikováno v:
Pigment International, Vol 8, Iss 3, Pp 179-185 (2021)
Bilateral segmental neurofibromatosis is a nonfamilial variant of neurofibromatosis without any systemic involvement. Speckled lentiginous nevus (SLN) is a pigmented, light brown to tan patch of varied diameter, speckled with smaller, darker colored
Externí odkaz:
https://doaj.org/article/7e612bd72b504697bf2f67a9a9d7e802
Publikováno v:
Medical Journal Armed Forces India. 79:356-359
Neurofibromatosis (NF) is an inherited neuroectodermal abnormality that primarily affects the growth of neural tissues, and Riccardi classified it into eight types. Segmental neurofibromatosis, which is a rare form of neurofibromatosis, is classified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1003cbd3815a7a7fb39e7b6a680deaf2
https://doi.org/10.1016/j.mjafi.2020.11.021
https://doi.org/10.1016/j.mjafi.2020.11.021
Autor:
Dufflart Ocampo, Juan David, Armendariz Barragan, Yonatan, Ruiz Gómez, Daniela, Sáenz Corral, Claudia Ileana, Toussaint Caire, Sonia, Vega Memije, Maria Elisa
Publikováno v:
CES Medicina, Volume: 36, Issue: 2, Pages: 140-147, Published: 04 OCT 2022
Resumen Introducción: la neurofibromatosis es un desorden genético, que afecta el crecimiento de tejidos neurales, con una incidencia de 1 en 4 000 personas, con impacto en la esperanza de vida por su asociación con neoplasias y enfermedad vascula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______618::5ef1839fc8ae2fb1f60e881db5dbaf12
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0120-87052022000200140&lng=en&tlng=en
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0120-87052022000200140&lng=en&tlng=en
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Neurofibromatosis (NF) are a group of genetic disorders that primarily affect neuroectoderm. It is a common disorder affecting 1 from 3000 persons. Since it is extremely variable in its presentation, Riccardi suggested in 1982 a useful system for cla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::bb63a02d524b4f84bb94917a09edd99d
https://www.bib.irb.hr/1220370
https://www.bib.irb.hr/1220370
Autor:
María Jesús Lobón-Iglesias, Ingrid Laurendeau, Michel Vidaud, Laurence Brugières, Eric Pasmant, Léa Guerrini-Rousseau, Arnault Tauziède-Espariat, Pascale Varlet, Audrey Briand-Suleau, Dominique Vidaud, Jacques Grill
Publikováno v:
Neuro-oncology Advances
Background Pediatric neurofibromatosis type 1 (NF1)–associated optic pathway gliomas (OPGs) exhibit different clinico-radiological features, treatment, and outcome compared with sporadic OPGs. While NF1-associated OPGs are caused by complete loss-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96e3dcc90e81518af07e9373535f5f45
https://doi.org/10.1093/noajnl/vdz054
https://doi.org/10.1093/noajnl/vdz054
Publikováno v:
Indian Journal of Dermatology, Vol 55, Iss 1, Pp 105-108 (2010)
Neurofibromatosis is a genetic disorder of neural crest-derived cells that primarily affect growth of neural tissues. It is broadly divided into three categories: (a) von Recklinghausen′s neurofibromatosis or NF-1, (b) bilateral acoustic neuroma (N
Externí odkaz:
https://doaj.org/article/c7f6994290cc491ebeacf6c52a395f08