Zobrazeno 1 - 10
of 302
pro vyhledávání: '"L, McGavran"'
Autor:
Bailleux, Sophie1 (AUTHOR), Cao, Sandrine2 (AUTHOR), Dezfoulian, Bita1 (AUTHOR), Collins, Patrick3 (AUTHOR), Somja, Joan3 (AUTHOR), Gatineau, Sophie4 (AUTHOR), Longton, Julie4 (AUTHOR), Nikkels, Arjen F.1 (AUTHOR) af.nikkels@uliege.be
Publikováno v:
Case Reports in Dermatology. Nov2024, Vol. 16 Issue 1, p248-253. 6p. 3 Illustrations.
Autor:
J, Wyatt-Ashmead, B K, Kleinschmidt-DeMasters, D A, Hill, G W, Mierau, L, McGavran, S J, Thompson, N K, Foreman
Publikováno v:
Clinical neuropathology. 20(6)
Rhabdoid phenotypic change has been described in a number of different neoplasms from diverse organ sites. These tumors share common light and electron-microscopic features, display a polyphenotypic immunohistochemical profile and often show cytogene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6dba934e15ae386a50a20e94b5372826
https://pubmed.ncbi.nlm.nih.gov/11758780
https://pubmed.ncbi.nlm.nih.gov/11758780
Publikováno v:
Medical and pediatric oncology. 34(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::97d77ab376d0c05d387d2e188c1033dc
https://pubmed.ncbi.nlm.nih.gov/10742076
https://pubmed.ncbi.nlm.nih.gov/10742076
Publikováno v:
Blood. 93(7)
Although numerous somatic mutations that contribute to the pathogenesis of childhood acute lymphoblastic leukemia (ALL) have been identified, no specific cytogenetic or molecular abnormalities are known to be consistently associated with relapse. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::59fdafde73d39fbd5eaf974f54476de2
https://pubmed.ncbi.nlm.nih.gov/10090949
https://pubmed.ncbi.nlm.nih.gov/10090949
Publikováno v:
British journal of haematology. 103(2)
The incidence of translocations involving the 11q23 gene MLL is markedly increased in leukaemias that occur in infants1 year of age. Epidemiological and molecular data have demonstrated that at least some of these translocations occur in utero. In th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b435da96792d96f70256b3a169a77dbf
https://pubmed.ncbi.nlm.nih.gov/9827932
https://pubmed.ncbi.nlm.nih.gov/9827932
Autor:
G A, Paskulin, G, Philips, R, Morgan, A, Sandberg, K, Richkind, C, Borovik, L, McGavran, N, Rabinovich, J, Dietz-Band, P, Erickson, H, Drabkin, M, Varella-Garcia
Publikováno v:
Genes, chromosomescancer. 21(2)
The 8;21 translocation in acute myeloid leukemia (AML) results in a consistent fusion transcript, AML1/ETO. Long-term clinical remission occurs in some patients despite incomplete eradication of AML1/ETO as demonstrated by RT-PCR, thus limiting the u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::650126439d0806f1ea7d294acef04b78
https://pubmed.ncbi.nlm.nih.gov/9491326
https://pubmed.ncbi.nlm.nih.gov/9491326
Publikováno v:
Genes, chromosomescancer. 20(4)
The t(1;19)(q23;p13), detected cytogenetically in 5-6% of cases, is one of the most common translocations in childhood acute lymphoblastic leukemia (ALL). Most t(1;19)+ ALLs are pseudodiploid or contain fewer than 50 chromosomes, are classified as pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::30444f135abc5f4694da57bc0b1c7da5
https://pubmed.ncbi.nlm.nih.gov/9408756
https://pubmed.ncbi.nlm.nih.gov/9408756
Publikováno v:
American journal of medical genetics. 62(4)
Hunter-McAlpine syndrome is an autosomal dominant disorder consisting of variable manifestations including craniosynostosis, almond-shaped palpebral fissures, small mouth, mild acral-skeletal anomalies, short stature, and mental deficiency. We report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c9c44eb55922a20a6ca645ba56c80da
https://pubmed.ncbi.nlm.nih.gov/8723067
https://pubmed.ncbi.nlm.nih.gov/8723067
Publikováno v:
Pediatric neurosurgery. 23(4)
A case of intracranial mixed malignant germ cell tumor (GCT) in a patient with the Klinefelter syndrome (KS) is reported. Extragonadal GCTs, including those of intracranial origin, have previously been noted in KS patients. A review of the English li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::60ebb8f40022dd61245e440af3c5678f
https://pubmed.ncbi.nlm.nih.gov/8835213
https://pubmed.ncbi.nlm.nih.gov/8835213
Publikováno v:
Obstetrics and gynecology. 82(2)
To obtain a timely fetal karyotype in selected circumstances by investigating the usefulness of fetal blood samples.Forty-five patients had fetal blood sampling for a variety of abnormalities including hydrocephalus, oligohydramnios, fetal growth ret
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e9d7f32b28c31ec31667cb005f4d790c
https://pubmed.ncbi.nlm.nih.gov/8336872
https://pubmed.ncbi.nlm.nih.gov/8336872