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Pediatric Neurology
|
September 1, 1990
Rett syndrome: findings suggesting axonopathy and mitochondrial abnormalities
S Wakai, K Kameda, Y Ishikawa, et al.
No to Hattatsu = Brain and Development
|
September 1, 1987
[Enlargement of the tongue and a deformity of the oral cavity in patients with Duchenne muscular dystrophy]
M Nagaoka, R Minami, S Wakai, et al.
Journal of Child Neurology
|
April 1, 1988
Peripheral neuropathy in four cases of group A xeroderma pigmentosum
N Tachi, K Sasaki, T Kusano, et al.
Epilepsia
|
July 1, 1994
Ictal video-EEG analysis of infantile neuroaxonal dystrophy
S Wakai, H Asanuma, H Hayasaka, et al.
Journal of Vascular Surgery
|
October 9, 2025
Cost-effectiveness analysis of surgical repair versus observation of complex abdominal aortic aneurysms in elderly patients
Hataka R Minami, Erin K Greenleaf, Besma J Nejim, et al.
Clinical Chemistry
|
October 6, 2000
A sensitive assay of tumor necrosis factor alpha in sera from Duchenne muscular dystrophy patients
K Saito, D Kobayashi, M Komatsu, et al.
Human Genetics
|
November 16, 1978
Prenatal diagnosis of GM1-gangliosidosis: biochemical manifestations in fetal tissues
T Kudoh, K Kikuchi, F Nakamura, et al.
Neurology
|
June 1, 1991
Delayed central conduction of somatosensory evoked potentials in xeroderma pigmentosum
T Imai, Y Ishikawa, R Minami, et al.
No to Hattatsu = Brain and Development
|
July 1, 1985
[Hereditary motor and sensory neuropathy type I in early childhood. Clinical features and the findings of nerve pathology]
N Tachi, Y Ishikawa, A Tsuzuki, et al.
European Journal of Pediatrics
|
November 1, 1981
Vitamin D dependent rickets: decreased sensitivity to 1,25-dihydroxyvitamin D
T Kudoh, T Kumagai, N Uetsuji, et al.
Page
of 19
Search research articles
Search
Showing results (131-140 of 184) with videos related to
Sort By:
Page
of 19
Pediatric Neurology
|
September 1, 1990
Rett syndrome: findings suggesting axonopathy and mitochondrial abnormalities
S Wakai, K Kameda, Y Ishikawa, et al.
No to Hattatsu = Brain and Development
|
September 1, 1987
[Enlargement of the tongue and a deformity of the oral cavity in patients with Duchenne muscular dystrophy]
M Nagaoka, R Minami, S Wakai, et al.
Journal of Child Neurology
|
April 1, 1988
Peripheral neuropathy in four cases of group A xeroderma pigmentosum
N Tachi, K Sasaki, T Kusano, et al.
Epilepsia
|
July 1, 1994
Ictal video-EEG analysis of infantile neuroaxonal dystrophy
S Wakai, H Asanuma, H Hayasaka, et al.
Journal of Vascular Surgery
|
October 9, 2025
Cost-effectiveness analysis of surgical repair versus observation of complex abdominal aortic aneurysms in elderly patients
Hataka R Minami, Erin K Greenleaf, Besma J Nejim, et al.
Clinical Chemistry
|
October 6, 2000
A sensitive assay of tumor necrosis factor alpha in sera from Duchenne muscular dystrophy patients
K Saito, D Kobayashi, M Komatsu, et al.
Human Genetics
|
November 16, 1978
Prenatal diagnosis of GM1-gangliosidosis: biochemical manifestations in fetal tissues
T Kudoh, K Kikuchi, F Nakamura, et al.
Neurology
|
June 1, 1991
Delayed central conduction of somatosensory evoked potentials in xeroderma pigmentosum
T Imai, Y Ishikawa, R Minami, et al.
No to Hattatsu = Brain and Development
|
July 1, 1985
[Hereditary motor and sensory neuropathy type I in early childhood. Clinical features and the findings of nerve pathology]
N Tachi, Y Ishikawa, A Tsuzuki, et al.
European Journal of Pediatrics
|
November 1, 1981
Vitamin D dependent rickets: decreased sensitivity to 1,25-dihydroxyvitamin D
T Kudoh, T Kumagai, N Uetsuji, et al.
Page
of 19