関: familial retinoblastoma、retinoblastoma、sporadic retinoblastoma

WordNet

malignant ocular tumor of retinal cells; usually occurs before the third year of life; composed of primitive small round retinal cells

PrepTutorEJDIC

世襲の,親譲りの / 遺伝的な,遺伝性の

UpToDate Contents

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1. 網膜芽細胞腫：臨床症状、評価、診断 retinoblastoma clinical presentation evaluation and diagnosis
2. 網膜芽細胞腫：治療と転帰 retinoblastoma treatment and outcome
3. 白色瞳孔を有する小児に対するアプローチ approach to the child with leukocoria
4. 軟部および骨肉腫の病原因子 pathogenetic factors in soft tissue and bone sarcomas
5. 放射線関連肉腫 radiation associated sarcomas

English Journal

Barley β-glucan accelerates wound healing by favoring migration versus proliferation of human dermal fibroblasts.

Fusté NP1, Guasch M1, Guillen P2, Anerillas C3, Cemeli T1, Pedraza N1, Ferrezuelo F1, Encinas M3, Moralejo M4, Garí E5.
Carbohydrate polymers.Carbohydr Polym.2019 Apr 15;210:389-398. doi: 10.1016/j.carbpol.2019.01.090. Epub 2019 Jan 28.
PMID 30732776

The Amazon Ocular Oncology Center: The first three years.

Cohen S1, Pretyman CS2, Sant'Ana R3, Singh N4, Morales M3, Belfort RN3.
Arquivos brasileiros de oftalmologia.Arq Bras Oftalmol.2019 Mar-Apr;82(2):107-110. doi: 10.5935/0004-2749.20190024. Epub 2019 Jan 24.
PMID 30698230

p53, stem cell biology and childhood blastomas.

Oh L1, Hafsi H2, Hainaut P2, Ariffin H1.
Current opinion in oncology.Curr Opin Oncol.2019 Mar;31(2):84-91. doi: 10.1097/CCO.0000000000000504.
PMID 30585860

Japanese Journal

頭頸部癌に対する遺伝子診断

耳鼻咽喉科臨床 110(6), 367-374, 2017
NAID 130005687773

希少がんの観点からみた遺伝性腫瘍症候群

腫瘍内科 = Clinical oncology 17(3), 316-332, 2016-03
NAID 40020773716

p53 Arg72Pro and MDM2 309 SNPs in hereditary retinoblastoma

Journal of human genetics 56(9), 685-686, 2011-09-01
NAID 10030661091

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Hereditary Retinoblastoma - St. Jude Children’s Research ...

Retinoblastoma is an eye cancer that typically develops in children before 5 years of age. ... What is retinoblastoma? Retinoblastoma is an eye cancer that typically develops in children before 5 years of age. This cancer develops in ...

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Malignant connective tissue tumors, particularly soft-tissue sarcomas and osteosarcomas, are recognized complications of hereditary retinoblastoma (1,2). An apparent high frequency of lipomas, which are benign tumors ...