4621. [Genetic aspects of leukemogenesis in mice (author's transl)].4622. [Juvenile polyposis coli--a case report (author's transl)].
作者: S Sato.;T Hirasawa.;H Imai.;M Tashiro.;M Numasawa.;H Wakasa.
来源: Nihon Shokakibyo Gakkai Zasshi. 1978年75卷4期545-51页 4623. [Chromosome aberrations in chronic myelogenous leukemia (author's transl)].4625. [Studies on a Japanese Burkitt lymphoma. Part 1. Establishment of a Japanese Burkitt lymphoma cell line (author's transl)].4626. [Aplastic anemia and acute leukemia in two siblings (author's transl)].
作者: F Sawa.;N Shinomiya.;S Maruyama.;T Nakagawa.;I Tsukimoto.;K Nakayama.
来源: Rinsho Ketsueki. 1978年19卷2期180-6页 4627. [A case of 45, X, -Y, Ph1 chronic granulocytic leukemia in an atomic bomb survivor and a review of the literature (author's transl)].4629. [Two cases of unusual extracolonic phenotypes accompanying familial polyposis of the colon--one with papillary carcinoma of the thyroid and the other with mesenteric fibromatosis (author's transl)].
作者: M Harada.;T Murakami.;Y Shishido.;R Hada.;S Itoh.;M Konn.;T Horimai.;H Fujita.
来源: Nihon Shokakibyo Gakkai Zasshi. 1977年74卷11期1567-74页 4632. [III. Leukemogenic factors and chromosome aberrations (author's transl)].4633. [Familial multiple hemangioblastomas--report of two cases in a family (author's transl)].
The authors reported their experience with two cases in a kindred with multiple hemangioblastomas in the cerebellum, brain stem, and spinal cord associated with von Hippel's disease, von Recklinghausen's disease and some visceral changes. (The members of this kindred died of similar disease.) Two patients, a 42-year-old man and his 14-year-old niece, showed various neurological signs involving central nervous system. Furthermore the man had some café-au-lait spots in the skin, a papillomatous tumors in the tongue and a vascular tumor in the right kidney. Both also had von Hippel's disease. Neuroradiological study and operations demonstrated multiple hemangioblastomas in the cerebellum, medulla oblongata and the spinal cord in association with abnormal enlargements of the medulla and the spinal cord which suggested coexistence of the parenchymatous tumor, probably glioma, in them. All hemangioblastomas in the cerebellum of both patients were removed. The literature of the familial multiple hemangioblastomas was reviewed and the coexistence of Lindau's disease, von Recklinghausen's disease and glioma was discussed.
4634. [Use of chromosomal findings in the treatment of acute myelogenous leukemia (author's transl)].4635. [Cytogenetic studies on leukemia with special reference to the relevance of chromosome abnormalities to the development of the disease (author's transl)].4636. [Cytogenetic study of tuberous sclerosis].4637. [Familial pheochromocytoma: four cases in one kindred (author's transl)].
作者: Y Mori.;H Kiyohara.;T Miki.;N Horiuchi.;T Kotake.
来源: Nihon Hinyokika Gakkai Zasshi. 1977年68卷4期398-406页 4638. [Follow-up investigation of retinoblastoma: Carcinogenesis and cancer (author's transl)].4640. [De Sanctis-Cacchione syndrome]. |