Myoung-Ja Park - JoVE Visualize

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Journal of Pediatric Surgery|March 24, 2009

Manifestation of alveolar rhabdomyosarcoma as primary cutaneous lesions in a neonate with Beckwith-Wiedemann syndromeMinoru Kuroiwa, Jun Sakamoto, Akira Shimada, et al.

Pediatric Blood & Cancer|August 24, 2010

NOTCH1 mutation in a female with myeloid/NK cell precursor acute leukemiaNorio Shiba, Takashi Kanazawa, Myoung-ja Park, et al.

[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|January 16, 2013

[Unrelated cord blood transplantation in a child with very severe aplastic anemia]Naoko Yasui, Katsuyoshi Koh, Myoung-Ja Park, et al.

International Journal of Hematology|December 17, 2013

Liver disease is frequently observed in Down syndrome patients with transient abnormal myelopoiesisMyoung Ja Park, Manabu Sotomatsu, Kentaro Ohki, et al.

International Journal of Hematology|January 4, 2021

Clinical features of 35 Down syndrome patients with transient abnormal myelopoiesis at a single institutionGenki Yamato, Myoung-Ja Park, Manabu Sotomatsu, et al.

Leukemia Research|October 24, 2006

Pro-inflammatory cytokinemia is frequently found in Down syndrome patients with hematological disordersAkira Shimada, Yasuhide Hayashi, Mizuho Ogasawara, et al.

Journal of Immunology (Baltimore, Md. : 1950)|June 26, 2012

Chronic mucocutaneous candidiasis caused by a gain-of-function mutation in the STAT1 DNA-binding domainShunichiro Takezaki, Masafumi Yamada, Masahiko Kato, et al.

British Journal of Haematology|February 28, 2009

FBXW7 and NOTCH1 mutations in childhood T cell acute lymphoblastic leukaemia and T cell non-Hodgkin lymphomaMyoung-Ja Park, Tomohiko Taki, Megumi Oda, et al.

Blood|December 6, 2011

CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML)Norio Shiba, Daisuke Hasegawa, Myoung-ja Park, et al.

Genes, Chromosomes & Cancer|January 24, 2007

Mutation and expression analyses of the MET and CDKN2A genes in rhabdomyosarcoma with emphasis on MET overexpressionYuyan Chen, Junko Takita, Masashi Mizuguchi, et al.

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Showing results (1-10 of 29) with videos related to

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Pageof 3

Journal of Pediatric Surgery|March 24, 2009

Manifestation of alveolar rhabdomyosarcoma as primary cutaneous lesions in a neonate with Beckwith-Wiedemann syndromeMinoru Kuroiwa, Jun Sakamoto, Akira Shimada, et al.

Pediatric Blood & Cancer|August 24, 2010

NOTCH1 mutation in a female with myeloid/NK cell precursor acute leukemiaNorio Shiba, Takashi Kanazawa, Myoung-ja Park, et al.

[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|January 16, 2013

[Unrelated cord blood transplantation in a child with very severe aplastic anemia]Naoko Yasui, Katsuyoshi Koh, Myoung-Ja Park, et al.

International Journal of Hematology|December 17, 2013

Liver disease is frequently observed in Down syndrome patients with transient abnormal myelopoiesisMyoung Ja Park, Manabu Sotomatsu, Kentaro Ohki, et al.

International Journal of Hematology|January 4, 2021

Clinical features of 35 Down syndrome patients with transient abnormal myelopoiesis at a single institutionGenki Yamato, Myoung-Ja Park, Manabu Sotomatsu, et al.

Leukemia Research|October 24, 2006

Pro-inflammatory cytokinemia is frequently found in Down syndrome patients with hematological disordersAkira Shimada, Yasuhide Hayashi, Mizuho Ogasawara, et al.

Journal of Immunology (Baltimore, Md. : 1950)|June 26, 2012

Chronic mucocutaneous candidiasis caused by a gain-of-function mutation in the STAT1 DNA-binding domainShunichiro Takezaki, Masafumi Yamada, Masahiko Kato, et al.

British Journal of Haematology|February 28, 2009

FBXW7 and NOTCH1 mutations in childhood T cell acute lymphoblastic leukaemia and T cell non-Hodgkin lymphomaMyoung-Ja Park, Tomohiko Taki, Megumi Oda, et al.

Blood|December 6, 2011

CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML)Norio Shiba, Daisuke Hasegawa, Myoung-ja Park, et al.

Genes, Chromosomes & Cancer|January 24, 2007

Mutation and expression analyses of the MET and CDKN2A genes in rhabdomyosarcoma with emphasis on MET overexpressionYuyan Chen, Junko Takita, Masashi Mizuguchi, et al.

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