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American Journal of Human Genetics
|
October 1, 1993
An A-to-G transition at nucleotide pair 11084 in the ND4 gene may be an mtDNA polymorphism
R Sakuta, Y Goto, I Nonaka, et al.
Brain & Development
|
July 1, 1991
Epidermal nevus syndrome with hemimegalencephaly: neuropathological study
R Sakuta, H Aikawa, S Takashima, et al.
Japanese Circulation Journal
|
December 1, 1986
The rapid diagnosis of group A streptococcal infection
I Seki, T Yabana, R Sakuta, et al.
Pediatric Neurology
|
May 1, 1993
Myopathy with abnormal distribution of dystrophin, growth retardation, mental retardation, and hypospadia
T Nagai, Y Tuchiya, A Maruyama, et al.
No to Hattatsu = Brain and Development
|
June 22, 2013
[Aspects of psychologists in the field of child neurology]
R Sakuta, Y Konishi, K Sugita, et al.
Annals of Neurology
|
March 1, 1993
Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
M Tokunaga, S Mita, R Sakuta, et al.
No to Hattatsu = Brain and Development
|
June 7, 2011
[Future perspectives of medical journals in pediatrics]
M Kaga, Y Sakakihara, N Shimizu, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
April 1, 1994
[Mitochondrial encephalomyopathy associated with parkinsonism and a point mutation in the mitochondrial tRNA(Leu)(UUR)) gene]
K Hara, M Yamamoto, T Anegawa, et al.
Brain & Development
|
January 1, 1989
Epidermal nevus syndrome with hemimegalencephaly: a clinical report of a case with acanthosis nigricans-like nevi on the face and neck, hemimegalencephaly, and hemihypertrophy of the body
R Sakuta, H Aikawa, S Takashima, et al.
No to Hattatsu = Brain and Development
|
February 24, 2001
[Decreased serotonin level in patients with anorexia nervosa]
R Sakuta, M Tazoe, N Narita, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 43) with videos related to
Sort By:
Page
of 5
American Journal of Human Genetics
|
October 1, 1993
An A-to-G transition at nucleotide pair 11084 in the ND4 gene may be an mtDNA polymorphism
R Sakuta, Y Goto, I Nonaka, et al.
Brain & Development
|
July 1, 1991
Epidermal nevus syndrome with hemimegalencephaly: neuropathological study
R Sakuta, H Aikawa, S Takashima, et al.
Japanese Circulation Journal
|
December 1, 1986
The rapid diagnosis of group A streptococcal infection
I Seki, T Yabana, R Sakuta, et al.
Pediatric Neurology
|
May 1, 1993
Myopathy with abnormal distribution of dystrophin, growth retardation, mental retardation, and hypospadia
T Nagai, Y Tuchiya, A Maruyama, et al.
No to Hattatsu = Brain and Development
|
June 22, 2013
[Aspects of psychologists in the field of child neurology]
R Sakuta, Y Konishi, K Sugita, et al.
Annals of Neurology
|
March 1, 1993
Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
M Tokunaga, S Mita, R Sakuta, et al.
No to Hattatsu = Brain and Development
|
June 7, 2011
[Future perspectives of medical journals in pediatrics]
M Kaga, Y Sakakihara, N Shimizu, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
April 1, 1994
[Mitochondrial encephalomyopathy associated with parkinsonism and a point mutation in the mitochondrial tRNA(Leu)(UUR)) gene]
K Hara, M Yamamoto, T Anegawa, et al.
Brain & Development
|
January 1, 1989
Epidermal nevus syndrome with hemimegalencephaly: a clinical report of a case with acanthosis nigricans-like nevi on the face and neck, hemimegalencephaly, and hemihypertrophy of the body
R Sakuta, H Aikawa, S Takashima, et al.
No to Hattatsu = Brain and Development
|
February 24, 2001
[Decreased serotonin level in patients with anorexia nervosa]
R Sakuta, M Tazoe, N Narita, et al.
Page
of 5