Factors affecting the intrusiveness and selection of real-site data collection methods in hot and humid climates: critical review

Autor: Moohialdin, Ammar, Lamari, Fiona, Miska, Marc, Trigunarsyah, Bambang

Publikováno v: Engineering, Construction and Architectural Management, 2020, Vol. 28, Issue 9, pp. 2300-2336.

Externí odkaz: http://www.emeraldinsight.com/doi/10.1108/ECAM-10-2019-0583

Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease—Report of New Cases

Autor: Ferran Celma Nos, Gonzalo Hernández, Xènia Ferrer-Cortès, Ines Hernandez-Rodriguez, Begoña Navarro-Almenzar, José Luis Fuster, Mar Bermúdez Cortés, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez

Publikováno v: International Journal of Molecular Sciences, Vol 22, Iss 11, p 5451 (2021)

Hereditary hyperferritinemia-cataract syndrome (HHCS) is a rare disease characterized by high serum ferritin levels, congenital bilateral cataracts, and the absence of tissue iron overload. This disorder is produced by mutations in the iron responsiv

Externí odkaz: https://doaj.org/article/c6c64e2c3b3d4d4fabe1a6a125f68892

Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease—Report of New Cases

Autor: José Luis Fuster, Ferran Celma Nos, Begoña Navarro-Almenzar, Ines Hernandez-Rodriguez, Xènia Ferrer-Cortès, Gonzalo Hernández, Mar Bermúdez Cortés, Santiago Pérez-Montero, Mayka Sanchez, Cristian Tornador

Publikováno v: International Journal of Molecular Sciences
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
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International Journal of Molecular Sciences, Vol 22, Iss 5451, p 5451 (2021)

Hereditary hyperferritinemia-cataract syndrome (HHCS) is a rare disease characterized by high serum ferritin levels, congenital bilateral cataracts, and the absence of tissue iron overload. This disorder is produced by mutations in the iron responsiv

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::987d28460d00ea7caf69ed4d420fbc46
http://europepmc.org/articles/PMC8196845

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Congenital Hyperferritinemia Diagnosed in A 2 Month Old-A Case Report from India

Autor: Lodh, Moushumi, Kerketta, Joshi Anand

Publikováno v: EJIFCC

Background In clinical medicine, ferritin is predominantly utilized as a serum marker of total body iron stores. In cases of iron deficiency and overload, serum ferritin serves a critical role in both diagnosis and management. Elevated serum and tiss

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::045bd4eebf8ff56c1a4b383a3494ade5
http://europepmc.org/articles/PMC4975243