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/vufind/Search/Results?lookfor=%22Moon%2C+Jung+Eun%22&type=Person&filter%5B%5D=topic_facet%3A%22Case+Reports%22
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PubPharm (6)
1
Metanephrine negative pheochromocytoma : a rare case report of dopamine-secreting tumor in an adolescent neurofibromatosis type 1 patient
enthalten in:
Annals of pediatric endocrinology & metabolism
| 2023
von
Lee, M.
|
Lee, R.
|
Park, S.
| +5
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2
A Korean male with Kleefstra syndrome presented with micropenis
enthalten in:
Annals of pediatric endocrinology & metabolism
| 2023
von
Lee, R.
|
Lee, M.
|
Moon, J.
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3
Case report of compound CFTR variants in Korean siblings with cystic fibrosis : importance of differentiating cystic fibrosis from inflammatory bowel disease
enthalten in:
Translational pediatrics
| 2021
von
Park, H.
|
Kim, J.
|
Choi, S.
| +7
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4
An Alport syndrome boy with Van Wyk-Grumbach syndrome induced by prolonged untreated congenital hypothyroidism
enthalten in:
Annals of pediatric endocrinology & metabolism
| 2020
von
Lee, S.
|
Moon, J.
|
Lee, G.
| +2
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5
Combined surgical and medical treatment in an adolescent with severe gynecomastia due to excessive estradiol secretion : a case report
enthalten in:
BMC pediatrics
| 2019
von
Moon, J.
|
Ko, C.
|
Yang, J.
| +1
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6
A de novo KMT2D mutation in a girl with Kabuki syndrome associated with endocrine symptoms : a case report
enthalten in:
BMC medical genetics
| 2018
von
Moon, J.
|
Lee, S.
|
Ko, C.
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1
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Thema: Case Reports
Medienart
6
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6
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6
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Zeitschriftentitel
3
Annals of pediatric endocrinology & metabolism
1
BMC medical genetics
1
BMC pediatrics
1
Translational pediatrics
Thema
Case Reports
2
Journal Article
1
2Z07MYW1AZ
1
4TI98Z838E
1
Alport syndrome
1
Anastrozole
1
Aromatase Inhibitors
1
CF transmembrane conductance regulator gene (CF...
1
Constitutional delay of puberty
1
Cystic fibrosis (CF)
1
DNA-Binding Proteins
1
Dopamine
1
EHMT1 gene
1
Estradiol
1
Excessive estradiol
1
Growth hormone deficiency
1
Hypothyroidism
1
KMT2D gene
1
KMT2D protein, human
1
Kabuki syndrome
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Erscheinungszeitraum
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2020-
2
2010-2019
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