Molecular characterization of galactokinase deficiency in Japanese patients
スポンサーリンク
概要
- 論文の詳細を見る
- 1999-11-01
著者
-
ASADA Minoru
Department of Adaptive Machine Systems, Graduate School of Engineering, Osaka University
-
Isshiki G
Osaka City Univ. Medical School Osaka Jpn
-
Isshiki Gen
Department Of Pediatrics Osaka City University
-
Suyama Itsujin
Osaka Municipal Rehabilitation Center For The Disabled
-
Okano Yoshiyuki
Department Of Pediatrics Osaka City University Graduate School Of Medicine
-
IMAMURA Takuji
Department of Pediatrics, Osaka City University Medical School
-
HASE Yutaka
Ikuno Public Health Center of Osaka City
-
HASE Yutaka
Osaka City Abeno Public Health Center
-
Imamura Takuji
Department Of Pediatrics Osaka City University Medical School
-
Imamura Takuji
Department Of Pediatrics Osaka City University Graduate School Of Medicine
-
Asada Minoru
Department Of Adaptive Machine Systems Graduate School Of Engineering Osaka University
-
Asada Minoru
Department Of Pediatrics Osaka City University Medical School
-
Okano Yoshiyuki
Department Of Pediatrics Osaka City Graduate School Of Medicine
関連論文
- Efficient Behavior Learning Based on State Value Estimation of Self and Others
- Wireless capsule endoscopy in pediatric patients : the first series from Japan
- Lexicon acquisition based on object-oriented behavior learning
- Usefulness of per-rectal portal scintigraphy with Tc-99m pertechnetate for galactosemia in infants
- Molecular characterization of galactokinase deficiency in Japanese patients
- Fetal Heart Malformations in Experimental in Hyperphenylalaninemia Pregnant Rats
- Histological findings in the livers of patients with neonatal intrahepatic cholestasis caused by citrin deficiency
- Molecular characterization of 6-pyruvoyl-tetrahydropterin synthase deficiency in Japanese patients
- Neopterin and biopterin concentrations in cerebrospinal fluid in controls less than 1 year old
- Control design principle of a low-cost humanoid system using a genetic algorithm
- Quantitative Analysis by X-Ray Diffraction of the Inclusion Complex Formed bd-Limonene in a β-Cyclodextrin/Maltodextrin Mixed Powder
- Enhanced continuous valued Q-learning for real autonomous robots
- Novel mutations, including the second most common in Japan, in the β-hexosaminidase α subunit gene, and a simple screening of Japanese patients with Tay-Sachs disease
- Diagnosis and treatment of 6-pyruvoyl-tetrahydropterin synthase deficiency
- Acquisition of joint attention through natural interaction utilizing motion cues
- Learning for joint attention helped by functional development
- Humanoid Robot Motion Recognition and Reproduction
- Poor Response to Substitution Therapy with Cortisone Acetate in Patients with Congenital Adrenal Hyperplasia
- Molecular characterization of phenylketonuria and tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency in Japan
- Mutation spectrum of and founder effects affecting the PTS gene in East Asian populations
- Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations
- Cross-sectional study of bone metabolism with nutrition in adult classical phenylketonuric patients diagnosed by neonatal screening
- Oxidative stress in patients with clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS)
- Subtelomeric deletions of 1q43q44 and severe brain impairment associated with delayed myelination
- Vowel Acquisition Based on an Auto-Mirroring Bias with a Less Imitative Caregiver