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/vufind/Search/Results?lookfor=%22Yasuda%2C+Kie%22&type=Person&sort=year
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PubPharm (16)
1
Comprehensive analyses of neurodevelopmental outcomes and quality of life of children with biliary atresia
enthalten in:
Journal of pediatric gastroenterology and nutrition
| 2024
von
Satomura, Y.
|
Tachibana, M.
|
Yasuda, K.
| +10
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2
Novel gene mutations in three Japanese patients with ARC syndrome associated mild phenotypes : a case series
enthalten in:
Journal of medical case reports
| 2022
von
Satomura, Y.
|
Bessho, K.
|
Nawa, N.
| +15
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3
Novel gene mutations in three Japanese patients with ARC syndrome associated mild phenotypes: a case series
enthalten in:
Journal of medical case reports
| 2022
von
Satomura, Y.
|
Bessho, K.
|
Nawa, N.
| +15
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4
Novel gene mutations in three Japanese patients with ARC syndrome associated mild phenotypes: a case series
enthalten in:
Journal of medical case reports
| 2022
von
Satomura, Y.
|
Bessho, K.
|
Nawa, N.
| +15
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5
Urinary iodine and thyroglobulin are useful markers in infants suspected of congenital hypothyroidism based on newborn screening
enthalten in:
Journal of pediatric endocrinology & metabolism : JPEM
| 2021
von
Tachibana, M.
|
Miyoshi, Y.
|
Fukui, M.
| +7
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6
Urinary iodine and thyroglobulin are useful markers in infants suspected of congenital hypothyroidism based on newborn screening
enthalten in:
The journal of pediatric endocrinology and metabolism
| 2021
von
Tachibana, M.
|
Miyoshi, Y.
|
Fukui, M.
| +7
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7
Urinary iodine and thyroglobulin are useful markers in infants suspected of congenital hypothyroidism based on newborn screening
enthalten in:
The journal of pediatric endocrinology and metabolism
| 2021
von
Tachibana, M.
|
Miyoshi, Y.
|
Fukui, M.
| +7
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8
An RNA aptamer restores defective bone growth in FGFR3-related skeletal dysplasia in mice
enthalten in:
Science translational medicine
| 2021
von
Kimura, T.
|
Bosakova, M.
|
Nonaka, Y.
| +21
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9
Two girls with a neonatal screening-negative 21-hydroxylase deficiency requiring treatment with hydrocortisone for virilization in late childhood
enthalten in:
Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
| 2021
von
Onuma, S.
|
Fukuoka, T.
|
Miyoshi, Y.
| +12
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10
CYP7A1 expression in hepatocytes is retained with upregulated fibroblast growth factor 19 in pediatric biliary atresia
enthalten in:
Hepatology research : the official journal of the Japan Society of Hepatology
| 2019
von
Hasegawa, Y.
|
Kawai, M.
|
Bessho, K.
| +11
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Medienart
16
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3
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Zeitschriftentitel
3
Clinical pediatric endocrinology : case reports...
3
Journal of medical case reports
2
Journal of pediatric gastroenterology and nutri...
2
The journal of pediatric endocrinology and meta...
1
Clinica chimica acta
1
Clinica chimica acta; international journal of ...
1
Hepatology Research
1
Hepatology research : the official journal of t...
1
Journal of pediatric endocrinology & metabolism...
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Thema
9
Journal Article
3
ARC syndrome
3
Mild phenotype
3
Neonatal cholestasis
3
Normal GGT
3
Severe hemorrhage
3
Targeted NGS
2
Bile Acids and Salts
2
Biomarkers
2
Case Reports
1
06LU7C9H1V
1
21-hydroxylase deficiency
1
3-hydroxy-3-methylglutaryl coenzyme A reductase
1
9002-71-5
1
9010-34-8
1
9679TC07X4
1
97C5T2UQ7J
1
Alagille Syndrome - metabolism
1
Alagille Syndrome - physiopathology
1
Alagille syndrome
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Erscheinungszeitraum
9
2020-
7
2010-2019
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Englisch
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