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PubPharm (75)
1
Clinical and genetic characteristics of three patients with congenital insensitivity to pain with anhidrosis : Case reports and a review of the literature
enthalten in:
Molecular genetics & genomic medicine
| 2024
von
Cho, J.
|
Hwang, S.
|
Kwak, Y.
| +11
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2
A 10-year follow-up of high-dose ambroxol treatment combined with enzyme replacement therapy for neuropathic Gaucher disease
enthalten in:
American journal of hematology
| 2024
von
Hwang, S.
|
Bae, H.
|
Yoon, J.
| +8
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3
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene
enthalten in:
Annals of pediatric endocrinology & metabolism
| 2024
von
Yoon, J.
|
Hwang, S.
|
Kim, J.
| +3
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4
Long-term endocrine sequelae after hematopoietic stem cell transplantation in children and adolescents
enthalten in:
Annals of pediatric endocrinology & metabolism
| 2024
von
Hwang, S.
|
Lee, Y.
|
Yoon, J.
| +6
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5
Impact of Early Diagnostic and Therapeutic Interventions and Clinical Course in Children and Adolescents with Multiple Endocrine Neoplasia Types 1 and 2
enthalten in:
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association
| 2024
von
Kim, J.
|
Lee, Y.
|
Hwang, S.
| +4
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6
Clinical and genetic characteristics of three patients with congenital insensitivity to pain with anhidrosis : Case reports and a review of the literature
enthalten in:
Molecular Genetics & Genomic Medicine
| 2024
von
Cho, J.
|
Hwang, S.
|
Kwak, Y.
| +11
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7
Clinical Characteristics and Long-Term Outcomes of Adrenal Tumors in Children and Adolescents
enthalten in:
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association
| 2023
von
Kim, J.
|
Choi, Y.
|
Hwang, S.
| +4
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8
Clinical outcomes and genotype-phenotype correlations in patients with complete and partial androgen insensitivity syndromes
enthalten in:
Annals of pediatric endocrinology & metabolism
| 2023
von
Lee, N.
|
Kim, J.
|
Yoon, J.
| +4
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9
Mutation spectrum and frequency of copy number variations of the ANOS1 gene in patients with Kallmann syndrome or normosmic isolated hypogonadotropic hypogonadism
enthalten in:
Endocrine connections
| 2023
von
Hye Kim, J.
|
Choi, Y.
|
Hwang, S.
| +6
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10
KBG syndrome : Clinical features and molecular findings in seven unrelated Korean families with a review of the literature
enthalten in:
Molecular genetics & genomic medicine
| 2023
von
Choi, Y.
|
Choi, J.
|
Do, H.
| +9
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Alzheimer’s disease
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cholesterol
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hempseed meal
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Drosophila Proteins
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Histone methylation
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