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PubPharm (35)
1
Muscle mass has a greater impact on serum creatinine levels in older males than in females
enthalten in:
Heliyon
| 2023
von
Yim, J.
|
Son, N.
|
Kyong, T.
| +2
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2
HPLC-MS/MS Method Validation for Antifungal Agents in Human Serum in Clinical Application
enthalten in:
Clinical laboratory
| 2023
von
Choi, H.
|
Yim, J.
|
Cha, J.
| +7
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3
A Case of X-Linked Adrenal Hypoplasia Congenital (AHC) Due to Large Deletion of NR0B1 (DAX1) and Contiguous Gene
enthalten in:
Annals of clinical and laboratory science
| 2023
von
Shin, C.
|
Kim, S.
|
Moon, C.
| +5
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4
Renal hypouricemia as the cause of exercise-induced acute kidney injury
enthalten in:
Kidney research and clinical practice
| 2023
von
Lee, H.
|
Kang, D.
|
Lee, H.
| +3
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5
CSF1R-related leukoencephalopathy with parkinsonism and dementia : functional neuroimaging findings
enthalten in:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
| 2023
von
Im, H.
|
Yoo, S.
|
Ye, B.
| +2
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6
CSF1R-related leukoencephalopathy with parkinsonism and dementia: functional neuroimaging findings
enthalten in:
Neurological sciences
| 2022
von
Im, H.
|
Yoo, S.
|
Ye, B.
| +2
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7
CSF1R-related leukoencephalopathy with parkinsonism and dementia: functional neuroimaging findings
enthalten in:
Neurological sciences
| 2022
von
Im, H.
|
Yoo, S.
|
Ye, B.
| +2
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8
Adrenocortical carcinoma and a sporadic MEN1 mutation in a 3-year-old girl : a case report
enthalten in:
Annals of pediatric endocrinology & metabolism
| 2022
von
Kim, S.
|
Lee, N.
|
Cho, W.
| +7
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9
18p Deletion Syndrome Originating from Rare Unbalanced Whole-Arm Translocation between Chromosomes 13 and 18 : A Case Report and Literature Review
enthalten in:
Children (Basel, Switzerland)
| 2022
von
Choi, J.
|
Moon, J.
|
Yoon, D.
| +3
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10
A Novel HNPP Phenotype in Charcot-Marie-Tooth Type 2E With c.1319C>T Missense Mutation in the NEFL Gene
enthalten in:
Journal of clinical neurology (Seoul, Korea)
| 2022
von
Choi, K.
|
Yim, J.
|
Kim, M.
| +1
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Ascorbic Acid
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Ascorbate Oxidase
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Cholesterol
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EC 1.10.3.3
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dysmorphic feature
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142M471B3J
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18p deletion syndrome
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304NUG5GF4
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4419T9MX03
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Erscheinungszeitraum
22
2020-
13
2010-2019
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