Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Miguel Gonzalez Santos"'
Publikováno v:
Galicia Clínica, Vol 83, Iss 4, Pp 60-63 (2022)
Hypokalemia, despite its potential seriousness, is frequently encountered in clinical practice; with the majority of cases occurring in adulthood being rationalized by examining the triad losses: diuretics, vomiting and diarrhea, as inherited causes
Externí odkaz:
https://doaj.org/article/d411ca035d414263adbeba45d48d829d
Autor:
Tatiana Pires, Catarina Duarte Santos, Miguel Gonzalez Santos, Luís Luz, Ana Ferrão, Maria J. Banza
Publikováno v:
European Journal of Case Reports in Internal Medicine (2021)
Eosinophilic granuloma is a localized, non-invasive form of Langerhans cell histiocytosis. It usually develops in the long bones and is more frequent in children under the age of 10 years. It is very rare in adults. We present the case of a young wom
Externí odkaz:
https://doaj.org/article/686b244fde5f4fc3b6c5bf456c51376e
Publikováno v:
European Journal of Case Reports in Internal Medicine
European Journal of Case Reports in Internal Medicine (2021)
European Journal of Case Reports in Internal Medicine (2021)
Ropivacaine is commonly used for post-operative pain management. We describe a case of neuroleptic malignant-like syndrome in a woman administered ropivacaine delivered using a drug infusion balloon. The presenting symptoms were confusion, agitation
Autor:
Maria J. Banza, Tatiana Costa Pires, Ana Ferrão, Miguel Gonzalez Santos, Catarina Duarte Santos, Luís Luz
Publikováno v:
European Journal of Case Reports in Internal Medicine (2021)
Eur J Case Rep Intern Med
Eur J Case Rep Intern Med
Eosinophilic granuloma is a localized, non-invasive form of Langerhans cell histiocytosis. It usually develops in the long bones and is more frequent in children under the age of 10 years. It is very rare in adults. We present the case of a young wom
Autor:
Rita Rodrigues, Miriam Magalhães, Tatiana Costa Pires, Catarina Santos, Miguel Gonzalez Santos, Alcina Ponte, Rita Lizardo Grácio
Publikováno v:
European Journal of Case Reports in Internal Medicine (2021)
Eur J Case Rep Intern Med
Eur J Case Rep Intern Med
Proteus syndrome is an extremely rare disorder that manifests as an asymmetric, disproportionate overgrowth of any connective tissue, such as bone, fat or epidermal nevi, in a mosaic or patchy pattern. It has an estimated prevalence of less than 1/1,
Publikováno v:
Visual Journal of Emergency Medicine. 27:101285
Autor:
Miguel Gonzalez-Santos, George B.J. Busby, Paolo Anagnostou, Cristian Capelli, Vincenzo Lorenzo Pascali, Erika Oosthuitzen, Ockie Oosthuitzen, Giovanni Destro-Bisol, Francesco Montinaro
Publikováno v:
Genetics
The characterization of the structure of southern African populations has been the subject of numerous genetic, medical, linguistic, archaeological, and anthropological investigations. Current diversity in the subcontinent is the result of complex ev
Autor:
Alessandro Raveane, Shahlo Turdikulova, Donata Luiselli, Pongsakorn Wangkumhang, Marta E. Alarcón-Riquelme, Francesco Montinaro, Guido Alberto Gnecchi-Ruscone, Damir Marjanović, Mait Metspalu, Sarabjit S. Mastana, Oleg Balanovsky, Alessandro Achilli, Antonio Torroni, Lejla Kovacevic, L. A. Atramentova, Anna Olivieri, Maria Fernanda Lima-Costa, Linda Ongaro, Cristian Capelli, Toomas Kivisild, Bernardo L. Horta, Nédio Mabunda, Marilia O. Scliar, Roy J. King, Etienne Patin, Kristiina Tambets, Garrett Hellenthal, Mauricio Lima Barreto, Celia A. May, Miguel Gonzalez-Santos, Andreja Leskovac, Andrés Moreno-Estrada, Eduardo Tarazona-Santos, Alexandre C. Pereira, Rodrigo Flores, Anastasia Kouvatsi, Luca Pagani, Stefania Sarno, Elena Balanovska, Ornella Semino, Davide Marnetto
Publikováno v:
Current Biology
Current Biology-CB
Current Biology-CB, 2019, 29 (23), pp.3974-3986.e4. ⟨10.1016/j.cub.2019.09.076⟩
Current Biology-CB, Elsevier, 2019, 29 (23), pp.3974-3986.e4. ⟨10.1016/j.cub.2019.09.076⟩
Current Biology-CB
Current Biology-CB, 2019, 29 (23), pp.3974-3986.e4. ⟨10.1016/j.cub.2019.09.076⟩
Current Biology-CB, Elsevier, 2019, 29 (23), pp.3974-3986.e4. ⟨10.1016/j.cub.2019.09.076⟩
The complexity of the admixture dynamics that shaped American populations is unveiled by Ongaro et al., where genetic data for more than 12,000 individuals from the continents are investigated. This study evaluates the dramatic impact of events after
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7305870a47c570d1863fdacb68c22310
https://hdl.handle.net/10668/14702
https://hdl.handle.net/10668/14702
Autor:
Alessandro Achilli, Shahlo Turdikulova, Miguel Gonzalez-Santos, Guido Alberto Gnecchi-Ruscone, Antonio Torroni, Celia A. May, Damir Marjanović, Cristian Capelli, Andrés Moreno-Estrada, Eduardo Tarazona-Santos, Linda Ongaro, Marta E. Alarcón-Riquelme, Bernardo L. Horta, Lejla Kovacevic, Anna Olivieri, Andreja Leskovac, Toomas Kivisild, L. A. Atramentova, Mait Metspalu, Alexandre C. Pereira, Alessandro Raveane, Elena Balanovska, Etienne Patin, Ornella Semino, Marilia O. Scliar, Anastasia Kouvatsi, Davide Marnetto, Kristiina Tambets, Rodrigo Flores, Luca Pagani, Maria Fernanda Lima-Costa, Francesco Montinaro, Stefania Sarno, Nédio Mabunda, Pongsakorn Wangkumhang, Roy J. King, Sarabjit S. Mastana, Oleg Balanovsky, Donata Luiselli, Garrett Hellenthal, Mauricio Lima Barreto
Publikováno v:
SSRN Electronic Journal.
The human genetic diversity of the Americas has been shaped by several events of gene flow that have continued since the Colonial Era and the Atlantic slave trade. Moreover, multiple waves of migration followed by local admixture occurred in the last
Autor:
Catarina Duarte Santos, Rita Lizardo Grácio, Tatiana Costa Pires, Miguel González Santos, Rita Jesus Rodrigues, Miriam Magalhães, Alcina Mota Ponte
Publikováno v:
European Journal of Case Reports in Internal Medicine (2021)
Proteus syndrome is an extremely rare disorder that manifests as an asymmetric, disproportionate overgrowth of any connective tissue, such as bone, fat or epidermal nevi, in a mosaic or patchy pattern. It has an estimated prevalence of less than 1/1,
Externí odkaz:
https://doaj.org/article/4a2036cec24f47cb87f7d03921e7fd86