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No to Hattatsu = Brain and Development
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July 1, 1989
[Two siblings of Leber's congenital amaurosis with an increase in very long chain fatty acid in blood: relationship between peroxisomal disorders and Leber's congenital amaurosis]
K Haginoya, J Aikawa, T Noro, et al.
The New England Journal of Medicine
|
March 10, 1983
An adult case of type Ib glycogen-storage disease. Enzymatic and histochemical studies
T Kuzuya, A Matsuda, S Yoshida, et al.
Pediatric Research
|
July 1, 1983
Glycogen storage disease type 1b: microsomal glucose-6-phosphatase system in two patients with different clinical findings
K Narisawa, H Otomo, Y Igarashi, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1983
Differential diagnosis of variant forms of hyperphenylalaninaemia by urinary pterins
H Hayakawa, K Narisawa, N Arai, et al.
Neuroscience Letters
|
June 29, 1988
Neurofilament degradation by bovine brain cathepsin D
H Suzuki, M Takeda, Y Nakamura, et al.
Journal of Gastroenterology and Hepatology
|
September 15, 1998
Three paediatric cases of primary sclerosing cholangitis treated with ursodeoxycholic acid and sulphasalazine
K Kozaiwa, H Tajiri, A Sawada, et al.
Dental Materials Journal
|
January 20, 1999
Cavity adaptation of resin composite in canine cavity in vivo
C Tani, K Itoh, M Ohba, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
May 1, 1990
An acute form of tyrosinemia type I with multiple intrahepatic mass lesions
Y Tazawa, M Kikuchi, I Kurobane, et al.
Japanese Journal of Ophthalmology
|
January 1, 1985
Gyrate atrophy of choroid and retina complicated by vitreous hemorrhage
O Takahashi, S Hayasaka, M Kiyosawa, et al.
The Tohoku Journal of Experimental Medicine
|
June 1, 1987
Regional cerebral metabolic rate for glucose and cerebrospinal fluid monoamine metabolites in subacute sclerosing panencephalitis
K Yanai, S Miyabayashi, K Iinuma, et al.
Page
of 63
Search research articles
Search
Showing results (401-410 of 623) with videos related to
Sort By:
Page
of 63
No to Hattatsu = Brain and Development
|
July 1, 1989
[Two siblings of Leber's congenital amaurosis with an increase in very long chain fatty acid in blood: relationship between peroxisomal disorders and Leber's congenital amaurosis]
K Haginoya, J Aikawa, T Noro, et al.
The New England Journal of Medicine
|
March 10, 1983
An adult case of type Ib glycogen-storage disease. Enzymatic and histochemical studies
T Kuzuya, A Matsuda, S Yoshida, et al.
Pediatric Research
|
July 1, 1983
Glycogen storage disease type 1b: microsomal glucose-6-phosphatase system in two patients with different clinical findings
K Narisawa, H Otomo, Y Igarashi, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1983
Differential diagnosis of variant forms of hyperphenylalaninaemia by urinary pterins
H Hayakawa, K Narisawa, N Arai, et al.
Neuroscience Letters
|
June 29, 1988
Neurofilament degradation by bovine brain cathepsin D
H Suzuki, M Takeda, Y Nakamura, et al.
Journal of Gastroenterology and Hepatology
|
September 15, 1998
Three paediatric cases of primary sclerosing cholangitis treated with ursodeoxycholic acid and sulphasalazine
K Kozaiwa, H Tajiri, A Sawada, et al.
Dental Materials Journal
|
January 20, 1999
Cavity adaptation of resin composite in canine cavity in vivo
C Tani, K Itoh, M Ohba, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
May 1, 1990
An acute form of tyrosinemia type I with multiple intrahepatic mass lesions
Y Tazawa, M Kikuchi, I Kurobane, et al.
Japanese Journal of Ophthalmology
|
January 1, 1985
Gyrate atrophy of choroid and retina complicated by vitreous hemorrhage
O Takahashi, S Hayasaka, M Kiyosawa, et al.
The Tohoku Journal of Experimental Medicine
|
June 1, 1987
Regional cerebral metabolic rate for glucose and cerebrospinal fluid monoamine metabolites in subacute sclerosing panencephalitis
K Yanai, S Miyabayashi, K Iinuma, et al.
Page
of 63