Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Pyknocytosis"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Christou Evangelos, Avgerinou Konstantina, Bachou Theodora, Douna Varvara, Mavrikou Mirsini, Delis Dimitris
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 5, Iss 3, Pp 130-132 (2020)
Infantile pyknocytosis (IP) is a rare cause of neonatal hemolytic disease. The exact etiology of this entity remains unclear. It is characterized by prolonged jaundice and transient hemolytic anemia, combined with increased proportion of pyknocytes i
Externí odkaz:
https://doaj.org/article/438c44dfd5684a0db675e36e7ae9fe27
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 2, Iss 1, Pp 81-84 (2013)
Infantile pyknocytosis is a rare form of neonatal haemolytic anaemia with unusual red cell morphology. Anaemia is mostly severe and red blood cells transfusion is often needed. In this report, we have described a male child aged 10 days, born at 37 w
Externí odkaz:
https://doaj.org/article/f0151b9b0e57488c926db80332830515
Autor:
Robert D. Christensen, Archana M. Agarwal, Mari C Knudsen, Timothy M. Bahr, Jessica Meznarich, Michell Lozano-Chinga, Robin K. Ohls
Publikováno v:
Biomedicine Hub
Biomedicine Hub, Vol 5, Iss 3, Pp 1-8 (2020)
Biomedicine Hub, Vol 5, Iss 3, Pp 1-8 (2020)
Infantile pyknocytosis is a rare, self-limited, hemolytic condition of unknown pathogenesis. It is diagnosed when a neonate with Coombs-negative hemolytic anemia has abundant pyknocytes and a characteristic clinical course after other hemolytic disor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db2074b36c2368ef90e886c4d2912f24
http://europepmc.org/articles/PMC8136318
http://europepmc.org/articles/PMC8136318
Autor:
Douna Varvara, Delis Dimitris, Avgerinou Konstantina, Bachou Theodora, Christou Evangelos, Mavrikou Mirsini
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 5, Iss 3, Pp 130-132 (2020)
Infantile pyknocytosis (IP) is a rare cause of neonatal hemolytic disease. The exact etiology of this entity remains unclear. It is characterized by prolonged jaundice and transient hemolytic anemia, combined with increased proportion of pyknocytes i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::569c90a4013b56824657fa9ebc685068
https://doi.org/10.1016/j.phoj.2020.06.007
https://doi.org/10.1016/j.phoj.2020.06.007
Publikováno v:
Journal of Pediatric Hematology/Oncology. 42:e251-e253
Infantile pyknocytosis is a rare cause of neonatal hemolytic anemia, which presents in the first few weeks of life. We report a classic case of infantile pyknocytosis that presented to our institution with rebound hyperbilirubinemia after receiving p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f9fff708e74454fd42bd9e84c69959d
https://doi.org/10.1097/mph.0000000000001461
https://doi.org/10.1097/mph.0000000000001461
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss 5, Pp 563-564 (2021)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5185f9748f26b864f30d2b15d63158e
https://pubmed.ncbi.nlm.nih.gov/34120867
https://pubmed.ncbi.nlm.nih.gov/34120867
Autor:
Alberto Berardi, Eleonora Balestri, Fabrizio Ferrari, Giovanni Palazzi, Claudio Chiossi, Goretta Bonacorsi, Eugenio Spaggiari
Publikováno v:
World Journal of Clinical Pediatrics
Infantile pyknocytosis (IP) is a rare, self-limited neonatal haemolytic anaemia that may require multiple blood transfusions. Only a little more than 50 cases have been reported in the medical literature, and the great majority of them concerns term
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c5c0395cc19e7254a6f8e03be2527aa
https://doi.org/10.5409/wjcp.v6.i4.176
https://doi.org/10.5409/wjcp.v6.i4.176
Publikováno v:
Journal of pediatric hematology/oncology. 43(7)
Infantile pyknocytosis is a rare and self-limiting cause of hemolytic anemia in neonates. It can result in severe anemia and hyperbilirubinemia. The pathogenesis is unknown: a genetic origin has been discussed; however, based on the current literatur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a4ae9b8272d985aff1708782252bd3d
https://pubmed.ncbi.nlm.nih.gov/33235153
https://pubmed.ncbi.nlm.nih.gov/33235153
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.