Zobrazeno 1 - 9
of 9
pro vyhledávání: '"David J. Ciske"'
Publikováno v:
Case Reports in Hematology, Vol 2021 (2021)
Central diabetes insipidus (CDI) is a rare reported complication of acute myeloid leukemia (AML). The onset of AML-associated CDI often precedes the diagnosis of AML by weeks or months and is considered an adverse prognostic indicator in this setting
Externí odkaz:
https://doaj.org/article/aa9b31eaf29b4cc0b49f0c7226803963
Publikováno v:
Case Reports in Hematology
Case Reports in Hematology, Vol 2021 (2021)
Case Reports in Hematology, Vol 2021 (2021)
Central diabetes insipidus (CDI) is a rare reported complication of acute myeloid leukemia (AML). The onset of AML-associated CDI often precedes the diagnosis of AML by weeks or months and is considered an adverse prognostic indicator in this setting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05617fed4bb1fdff97bc065171056c98
https://doi.org/10.1155/2021/8898671
https://doi.org/10.1155/2021/8898671
Publikováno v:
The American Journal of Medicine. 133:e13-e14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::853ec7086a70d8cb9d0849232f924393
https://doi.org/10.1016/j.amjmed.2019.07.006
https://doi.org/10.1016/j.amjmed.2019.07.006
Publikováno v:
Pediatrics. 107:699-705
Objective. To assess the effectiveness of communication between health care providers (physicians, nurses, genetic counselors) in Wisconsin and parents of children identified as heterozygote carriers for cystic fibrosis (CF) in the routine Wisconsin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5e3fa42d92e35b349f2f8e7d5a568ec
https://doi.org/10.1542/peds.107.4.699
https://doi.org/10.1542/peds.107.4.699
Publikováno v:
American Journal of Medical Genetics. 98:313-316
Neuroectodermal melanolysosomal disease, also known as Elejalde syndrome, is a rare syndrome characterized by silvery hair, pigment abnormalities, and profound central nervous system dysfunction. It is similar to the Chediak-Higashi and Griscelli syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67c3094b64e9c3510b0ff212f1c31d64
https://doi.org/10.1002/1096-8628(20010201)98:4<313::aid-ajmg1098>3.0.co
https://doi.org/10.1002/1096-8628(20010201)98:4<313::aid-ajmg1098>3.0.co
Publikováno v:
American Journal of Medical Genetics. 82:301-304
The Nager syndrome is the most common form of acrofacial dysostosis. Although autosomal dominant and recessive forms of acrofacial dysostosis have been described the molecular etiology of these disorders is unknown. We report on a child with acrofaci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90e686e2e162146704afb27e1a1de939
https://doi.org/10.1002/(sici)1096-8628(19990212)82:4<301::aid-ajmg5>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19990212)82:4<301::aid-ajmg5>3.0.co
Autor:
Paul G. McGovern, Wei Zheng, Lawrence H. Kushi, Thomas A. Sellers, V. Elving Anderson, Celine M. Vachon, Stephen S. Rich, Sue A. Bartow, Richard A. King, David J. Ciske
Publikováno v:
Genetic Epidemiology. 13:317-328
Most segregation analyses of breast cancer susceptibility have modeled the effect of the major gene on the age-at-onset distribution. However, in families linked to BRCA1 or BRCA2, there is wide variation in the age-at-onset among gene carriers. We p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa69def94a50dfa6bf55f9f92967b38c
https://doi.org/10.1002/(sici)1098-2272(1996)13:4<317::aid-gepi1>3.0.co
https://doi.org/10.1002/(sici)1098-2272(1996)13:4<317::aid-gepi1>3.0.co
Publikováno v:
American Journal of Medical Genetics. 75:59-61
Chondrodysplasia punctata (CDP) is associated with a variety of genetic and nongenetic conditions. We report a girl with CDP, complex congenital cardiac disease, central nervous system (CNS) anomalies, and clinical findings that resemble those of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20b163fbae63f00066be18c3873b7526
https://doi.org/10.1002/(sici)1096-8628(19980106)75:1<59::aid-ajmg13>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19980106)75:1<59::aid-ajmg13>3.0.co
Publikováno v:
The American journal of medicine. 107(1)
Recent genetic research has isolated the primary genetic defect underlying many of the hereditary colorectal cancer syndromes. Obtaining a detailed family history is the first step in identifying individuals at increased risk of developing colorectal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9e8c20fd7fba9071c2a10252cd5e0ec
https://pubmed.ncbi.nlm.nih.gov/10403355
https://pubmed.ncbi.nlm.nih.gov/10403355