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Rinsho Shinkeigaku = Clinical Neurology
|
August 1, 1997
[A family with facioscapulohumeral muscular dystrophy and hereditary long QT syndrome]
T Kimura, T Moriwaki, J Sawada, et al.
Transplantation Proceedings
|
May 8, 2018
Desensitization with the Use of an Antibody Removal-Free Protocol in ABO-Incompatible Kidney Transplant Recipients with a Low Anti-A/B Antibody Titer
K Nanmoku, T Shinzato, T Kubo, et al.
Microbiology (Reading, England)
|
October 28, 1999
Genetic organization and characteristics of the 3-(3-hydroxyphenyl)propionic acid degradation pathway of Comamonas testosteroni TA441
H Arai, T Yamamoto, T Ohishi, et al.
Pathology International
|
June 10, 2000
Clear cell sarcoma arising in the transverse colon
T Fukuda, T Kakihara, K Baba, et al.
Internal Medicine (Tokyo, Japan)
|
September 1, 1996
Hemolytic anemia associated with myotonic muscular dystrophy
T Komeno, H Ninomiya, T Itoh, et al.
Journal of Dental Research
|
December 24, 2004
Hyper-expression of osteocalcin mRNA in odontoblasts of Hyp mice
T Onishi, T Ogawa, T Hayashibara, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene
|
May 1, 1992
Detection of circulating antigens in human trichinellosis
T Nishiyama, T Araki, N Mizuno, et al.
Surgical Oncology
|
December 1, 1993
Nucleolar organizer regions are independently associated with a shortened survival in patients with non-small cell lung cancer
T Oyama, T Mitsudomi, Y Yoshida, et al.
Acta Neurochirurgica
|
January 1, 1997
Loss and apoptosis of smooth muscle cells in intracranial aneurysms. Studies with in situ DNA end labeling and antibody against single-stranded DNA
T Sakaki, E Kohmura, T Kishiguchi, et al.
Hepato-Gastroenterology
|
February 1, 1994
Biliary diverticulum with pancreaticobiliary maljunction
Y Ikematsu, T Eto, T Tomioka, et al.
Page
of 218,495
Search research articles
Search
Showing results (171-180 of 2,184,945) with videos related to
Sort By:
Page
of 218,495
Rinsho Shinkeigaku = Clinical Neurology
|
August 1, 1997
[A family with facioscapulohumeral muscular dystrophy and hereditary long QT syndrome]
T Kimura, T Moriwaki, J Sawada, et al.
Transplantation Proceedings
|
May 8, 2018
Desensitization with the Use of an Antibody Removal-Free Protocol in ABO-Incompatible Kidney Transplant Recipients with a Low Anti-A/B Antibody Titer
K Nanmoku, T Shinzato, T Kubo, et al.
Microbiology (Reading, England)
|
October 28, 1999
Genetic organization and characteristics of the 3-(3-hydroxyphenyl)propionic acid degradation pathway of Comamonas testosteroni TA441
H Arai, T Yamamoto, T Ohishi, et al.
Pathology International
|
June 10, 2000
Clear cell sarcoma arising in the transverse colon
T Fukuda, T Kakihara, K Baba, et al.
Internal Medicine (Tokyo, Japan)
|
September 1, 1996
Hemolytic anemia associated with myotonic muscular dystrophy
T Komeno, H Ninomiya, T Itoh, et al.
Journal of Dental Research
|
December 24, 2004
Hyper-expression of osteocalcin mRNA in odontoblasts of Hyp mice
T Onishi, T Ogawa, T Hayashibara, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene
|
May 1, 1992
Detection of circulating antigens in human trichinellosis
T Nishiyama, T Araki, N Mizuno, et al.
Surgical Oncology
|
December 1, 1993
Nucleolar organizer regions are independently associated with a shortened survival in patients with non-small cell lung cancer
T Oyama, T Mitsudomi, Y Yoshida, et al.
Acta Neurochirurgica
|
January 1, 1997
Loss and apoptosis of smooth muscle cells in intracranial aneurysms. Studies with in situ DNA end labeling and antibody against single-stranded DNA
T Sakaki, E Kohmura, T Kishiguchi, et al.
Hepato-Gastroenterology
|
February 1, 1994
Biliary diverticulum with pancreaticobiliary maljunction
Y Ikematsu, T Eto, T Tomioka, et al.
Page
of 218,495