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Quoted phrase not found in phrase index: "Ring chromosome anomaly"
Page 1
Postleukemic dysmyelopoiesis.
Foucar K, Vaughan WP, Armitage JO, Patil S, Dick F, Karp JE. Foucar K, et al. Am J Hematol. 1983 Dec;15(4):321-34. doi: 10.1002/ajh.2830150403. Am J Hematol. 1983. PMID: 6650493
This period of prolonged dyspoiesis was not associated with rising myeloblast counts or clinical evidence of relapse. Dyspoietic abnormalities developed while two patients were receiving maintenance chemotherapy; the other two patients received no maintenance therap …
This period of prolonged dyspoiesis was not associated with rising myeloblast counts or clinical evidence of relapse. Dyspoietic a …
The phenotype and rhGH treatment response of ring Chromosome 15 Syndrome: Case report and literature review.
Chen M, Ke X, Liang H, Gong F, Yang H, Wang L, Duan L, Pan H, Cao D, Zhu H. Chen M, et al. Mol Genet Genomic Med. 2021 Dec;9(12):e1842. doi: 10.1002/mgg3.1842. Epub 2021 Nov 8. Mol Genet Genomic Med. 2021. PMID: 34747577 Free PMC article. Review.
BACKGROUND: Ring chromosome 15 [r (15)] is an uncommon finding with various clinical manifestations. ...The height has increased 3.8 cm (+0.2SDS) and the calculated growth rate has improved from 4.7 to 7.6 cm/y. The literature review indicated the main cli …
BACKGROUND: Ring chromosome 15 [r (15)] is an uncommon finding with various clinical manifestations. ...The height has …
Therapy-related leukemia: a panmyelosis.
Foucar K, McKenna RW, Bloomfield CD, Bowers TK, Brunning RD. Foucar K, et al. Cancer. 1979 Apr;43(4):1285-96. doi: 10.1002/1097-0142(197904)43:4<1285::aid-cncr2820430416>3.0.co;2-j. Cancer. 1979. PMID: 445330
Neutrophilic and erythroid abnormalities were most striking in 12 of the patients, megakaryocytic abnormalities predominated in 2 and monocytic abnormalities in 1. ...All of the 7 patients who had bone marrow chromosome studies exhibited major chromoso …
Neutrophilic and erythroid abnormalities were most striking in 12 of the patients, megakaryocytic abnormalities predominated i …
Apparent mineralocorticoid excess: type I and type II.
Mantero F, Palermo M, Petrelli MD, Tedde R, Stewart PM, Shackleton CH. Mantero F, et al. Steroids. 1996 Apr;61(4):193-6. doi: 10.1016/0039-128x(96)00012-8. Steroids. 1996. PMID: 8732999 Review.
The biochemical marker of this disorder is an increased ratio of tetrahydrocortisol (THF) + allo-THF/tetrahydrocortisone (THE) in the urine, which has been found in more than 20 patients described to date, together with evidence of a more general defect in steroid ring A r …
The biochemical marker of this disorder is an increased ratio of tetrahydrocortisol (THF) + allo-THF/tetrahydrocortisone (THE) in the urine, …
Chromosome studies in 500 induced abortions.
Yamamoto M, Fujimori R, Ito T, Kamimura K, Watanabe G. Yamamoto M, et al. Humangenetik. 1975 Aug 29;29(1):9-14. doi: 10.1007/BF00273345. Humangenetik. 1975. PMID: 1176132
Neither satellited nor small chromosomes were predominantly involved in the formation of chromosome anomalies. ...Trisomies were virtually found at random, regardless of the chromosomal characteristics. Satellite clusters and smaller chromosomes …
Neither satellited nor small chromosomes were predominantly involved in the formation of chromosome anomalies. ...Triso …
Wilson's disease in Eastern India.
Sinha S, Jha DK, Sinha KK. Sinha S, et al. J Assoc Physicians India. 2001 Sep;49:881-4. J Assoc Physicians India. 2001. PMID: 11837754
AIM: The aim is to study the clinical features, biochemical and radiological abnormalities of this disorder in Eastern India and the effect of treatment. ...They commonly presented with dysarthria, dystonia or drooling. The clinical features were dystonia (96 …
AIM: The aim is to study the clinical features, biochemical and radiological abnormalities of this disorder in Eastern India a …
Epilepsy-related brain networks in ring chromosome 20 syndrome: an EEG-fMRI study.
Vaudano AE, Ruggieri A, Vignoli A, Avanzini P, Benuzzi F, Gessaroli G, Nichelli PF, Darra F, Cantalupo G, Mastrangelo M, Dalla Bernardina B, Canevini MP, Meletti S. Vaudano AE, et al. Epilepsia. 2014 Mar;55(3):403-13. doi: 10.1111/epi.12539. Epub 2014 Jan 31. Epilepsia. 2014. PMID: 24483620 Free article.
OBJECTIVE: To identify the brain networks that are involved in the different electroencephalography (EEG) abnormalities in patients with ring chromosome 20 [r(20)] syndrome. We hypothesize the existence of both distinctive and common brain circuits for the pa …
OBJECTIVE: To identify the brain networks that are involved in the different electroencephalography (EEG) abnormalities in patients w …
Peculiarities of abnormal karyotypes formation in therapy-related acute leukemias.
Andreieva SV, Kyselova OA, Serbin IM, Alkhimova OG. Andreieva SV, et al. Exp Oncol. 2020 Jun;42(2):126-129. doi: 10.32471/exp-oncology.2312-8852.vol-42-no-2.14593. Exp Oncol. 2020. PMID: 32602288
AIM: To determine ways of formation of abnormal karyotypes in two clinical cases of secondary acute leukemias of myeloid and lymphoid lineages. ...RESULTS: An unusually large number of quantitative and structural anomalies of chromosomes in therapy-related ac …
AIM: To determine ways of formation of abnormal karyotypes in two clinical cases of secondary acute leukemias of myeloid and lymphoid …
Ring chromosome may signal progression of Fanconi anemia.
Abdelgadir RE, Mohamed K, Elmula IF. Abdelgadir RE, et al. Gulf J Oncolog. 2016 Sep;1(22):43-46. Gulf J Oncolog. 2016. PMID: 28191805
However, another patient without ring chromosome developed AML after 23 months of the diagnosis. BM analysis showed non-random clonal chromosomal abnormalities such as del (20) (q11) in 3 cases; add(1)(q12); -7, -8, and +9 in one case each. Normal kary …
However, another patient without ring chromosome developed AML after 23 months of the diagnosis. BM analysis showed non-ran …
The ring chromosome 13 syndrome.
Martin NJ, Harvey PJ, Pearn JH. Martin NJ, et al. Hum Genet. 1982;61(1):18-23. doi: 10.1007/BF00291324. Hum Genet. 1982. PMID: 7129419
A study of the ring chromosome 13 syndrome is presented with detailed clinical and cytogenetic features of three new unrelated cases. ...Peripheral blood cultures showed an average of 88% of metaphases to be 46,XX,r(13), with the remaining 12% manifesting eit …
A study of the ring chromosome 13 syndrome is presented with detailed clinical and cytogenetic features of three new un …
40 results