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Mamiko Yamada

Showing results (21-30 of 86) with videos related to

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Pediatric Nephrology (Berlin, Germany)|February 8, 2024
SALL4 deletion and kidney and cardiac defects associated with VACTERL associationDaisuke Watanabe, Daisuke Nakato, Mamiko Yamada, et al.
Internal Medicine (Tokyo, Japan)|August 8, 2017
Histological Changes in Autoimmune Hepatitis with Graves' Disease: A Child Case ReportMamiko Yamada, Hironori Shibata, Yohei Masugi, et al.
Congenital Anomalies|October 29, 2020
Role of chimeric transcript formation in the pathogenesis of birth defectsMamiko Yamada, Hisato Suzuki, Akiko Watanabe, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 14, 2023
Café-au-lait Spots and Cleft Palate: Not a Chance AssociationMamiko Yamada, Katsumi Tanito, Hisato Suzuki, et al.
Journal of Medical Ultrasonics (2001)|June 10, 2016
Marked change in Doppler waveform: report of two cases of subcutaneous hematomaTakako Watanabe, Hideaki Ishida, Tomoya Komatsuda, et al.
Journal of Medical Ultrasonics (2001)|June 10, 2016
Isolated liver metastasis from a renal cell carcinoma 12 years after nephrectomy: report of a case and literature reviewHideo Ohno, Hideaki Ishida, Tomoya Komatsuda, et al.
American Journal of Medical Genetics. Part A|December 31, 2020
Biallelic loss of OTUD7A causes severe muscular hypotonia, intellectual disability, and seizuresHisato Suzuki, Mie Inaba, Mamiko Yamada, et al.
European Journal of Medical Genetics|June 10, 2024
Biallelic loss-of-function variants in the centriolar protein CCP110 leads to a ciliopathy-like phenotypeHisato Suzuki, Yukako Muramatsu, Fuyuki Miya, et al.
American Journal of Medical Genetics. Part A|March 9, 2019
SATB2-associated syndrome in patients from Japan: Linguistic profilesMamiko Yamada, Tomoko Uehara, Hisato Suzuki, et al.
American Journal of Medical Genetics. Part A|May 16, 2020
Shortfall of exome analysis for diagnosis of Shwachman-Diamond syndrome: Mismapping due to the pseudogene SBDSP1Mamiko Yamada, Tomoko Uehara, Hisato Suzuki, et al.
Pageof 9

Showing results (21-30 of 86) with videos related to

Sort By:
Pageof 9
Pediatric Nephrology (Berlin, Germany)|February 8, 2024
SALL4 deletion and kidney and cardiac defects associated with VACTERL associationDaisuke Watanabe, Daisuke Nakato, Mamiko Yamada, et al.
Internal Medicine (Tokyo, Japan)|August 8, 2017
Histological Changes in Autoimmune Hepatitis with Graves' Disease: A Child Case ReportMamiko Yamada, Hironori Shibata, Yohei Masugi, et al.
Congenital Anomalies|October 29, 2020
Role of chimeric transcript formation in the pathogenesis of birth defectsMamiko Yamada, Hisato Suzuki, Akiko Watanabe, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 14, 2023
Café-au-lait Spots and Cleft Palate: Not a Chance AssociationMamiko Yamada, Katsumi Tanito, Hisato Suzuki, et al.
Journal of Medical Ultrasonics (2001)|June 10, 2016
Marked change in Doppler waveform: report of two cases of subcutaneous hematomaTakako Watanabe, Hideaki Ishida, Tomoya Komatsuda, et al.
Journal of Medical Ultrasonics (2001)|June 10, 2016
Isolated liver metastasis from a renal cell carcinoma 12 years after nephrectomy: report of a case and literature reviewHideo Ohno, Hideaki Ishida, Tomoya Komatsuda, et al.
American Journal of Medical Genetics. Part A|December 31, 2020
Biallelic loss of OTUD7A causes severe muscular hypotonia, intellectual disability, and seizuresHisato Suzuki, Mie Inaba, Mamiko Yamada, et al.
European Journal of Medical Genetics|June 10, 2024
Biallelic loss-of-function variants in the centriolar protein CCP110 leads to a ciliopathy-like phenotypeHisato Suzuki, Yukako Muramatsu, Fuyuki Miya, et al.
American Journal of Medical Genetics. Part A|March 9, 2019
SATB2-associated syndrome in patients from Japan: Linguistic profilesMamiko Yamada, Tomoko Uehara, Hisato Suzuki, et al.
American Journal of Medical Genetics. Part A|May 16, 2020
Shortfall of exome analysis for diagnosis of Shwachman-Diamond syndrome: Mismapping due to the pseudogene SBDSP1Mamiko Yamada, Tomoko Uehara, Hisato Suzuki, et al.
Pageof 9