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Phuc Nguyen

Showing results (461-470 of 482) with videos related to

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Scientific Data|March 29, 2024
BM-BronchoLC - A rich bronchoscopy dataset for anatomical landmarks and lung cancer lesion recognitionVan Giap Vu, Anh Duc Hoang, Thu Phuong Phan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 20, 2022
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2023
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
Zeitschrift Fur Gastroenterologie|April 11, 2023
Michael Bitzer, Sabrina Groß, Jörg Albert, et al.
Zeitschrift Fur Gastroenterologie|April 11, 2023
Michael Bitzer, Sabrina Groß, Jörg Albert, et al.
Zeitschrift Fur Gastroenterologie|February 16, 2024
Michael Bitzer, Sabrina Groß, Jörg Albert, et al.
Zeitschrift Fur Gastroenterologie|January 9, 2024
Sabrina Groß, Michael Bitzer, Jörg Albert, et al.
Zeitschrift Fur Gastroenterologie|February 16, 2024
Sabrina Groß, Michael Bitzer, Jörg Albert, et al.
Zeitschrift Fur Gastroenterologie|January 9, 2024
Michael Bitzer, Sabrina Groß, Jörg Albert, et al.
Zeitschrift Fur Gastroenterologie|March 10, 2025
Michael Bitzer, Sabrina Groß, Jörg Albert, et al.
Pageof 49

Showing results (461-470 of 482) with videos related to

Sort By:
Pageof 49
Scientific Data|March 29, 2024
BM-BronchoLC - A rich bronchoscopy dataset for anatomical landmarks and lung cancer lesion recognitionVan Giap Vu, Anh Duc Hoang, Thu Phuong Phan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 20, 2022
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2023
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
Zeitschrift Fur Gastroenterologie|April 11, 2023
Michael Bitzer, Sabrina Groß, Jörg Albert, et al.
Zeitschrift Fur Gastroenterologie|April 11, 2023
Michael Bitzer, Sabrina Groß, Jörg Albert, et al.
Zeitschrift Fur Gastroenterologie|February 16, 2024
Michael Bitzer, Sabrina Groß, Jörg Albert, et al.
Zeitschrift Fur Gastroenterologie|January 9, 2024
Sabrina Groß, Michael Bitzer, Jörg Albert, et al.
Zeitschrift Fur Gastroenterologie|February 16, 2024
Sabrina Groß, Michael Bitzer, Jörg Albert, et al.
Zeitschrift Fur Gastroenterologie|January 9, 2024
Michael Bitzer, Sabrina Groß, Jörg Albert, et al.
Zeitschrift Fur Gastroenterologie|March 10, 2025
Michael Bitzer, Sabrina Groß, Jörg Albert, et al.
Pageof 49