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PubPharm (337)
1
Atypical mandibulofacial dysostosis with microcephaly diagnosed through the identification of a novel pathogenic mutation in EFTUD2
enthalten in:
Molecular genetics & genomic medicine
| 2024
von
Chen, Y.
|
Yang, R.
|
Chen, X.
| +7
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2
Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient : a case report
enthalten in:
Annals of hematology
| 2024
von
Zhang, J.
|
Chen, H.
|
Ruan, D.
| +12
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3
Link between mutations in ACVRL1 and PLA2G4A genes and chronic intestinal ulcers : A case report and review of literature
enthalten in:
World journal of gastrointestinal surgery
| 2024
von
Tang, Y.
|
Zhang, J.
|
Wang, J.
| +7
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4
Dacryocystocele and Subsequent Dacryocystectomy in a Patient With Bosma Arhinia Microphthalmia Syndrome (BAMS) : A Case Report and Review of Literature
enthalten in:
Journal of pediatric ophthalmology and strabismus
| 2024
von
Stenz, E.
|
Nyalakonda, R.
|
McCulley, T.
| +1
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5
The use of sertraline to treat an adolescent of dystonia comorbid with major depressive disorder with psychotic features
enthalten in:
Neuropsychopharmacology reports
| 2024
von
Liu, C.
|
Lan, C.
|
Chen, Y.
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6
Resolving unexpected ABO typing discrepancies in two patients
enthalten in:
Transfusion medicine (Oxford, England)
| 2024
von
Yen, K.
|
Chen, S.
|
Chen, Y.
| +2
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7
A case report on multiple acyl-CoA dehydrogenase deficiency with severe myopathy and osteoporosis
enthalten in:
International journal of rheumatic diseases
| 2024
von
Li, M.
|
Lin, Z.
|
Chen, Y.
| +3
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8
Does the Dose of Standard Adjuvant Chemotherapy Affect the Triple-negative Breast Cancer Benefit from Extended Capecitabine Metronomic Therapy? An Exploratory Analysis of the SYSUCC-001 Trial
enthalten in:
Breast cancer (Dove Medical Press)
| 2024
von
Chen, Y.
|
Li, W.
|
Wu, J.
| +38
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9
Prefabricated Zirconia Crowns and Preformed Metal Crowns in the Treatment of Severely Childhood Caries and Anterior Crossbite in a Child with Autistic Spectrum Disorder
enthalten in:
Case reports in dentistry
| 2024
von
Deng, S.
|
Gao, Q.
|
Zhang, L.
| +3
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10
Identification and characterization of a novel CASR mutation causing familial hypocalciuric hypercalcemia
enthalten in:
Frontiers in endocrinology
| 2024
von
Lin, C.
|
Ding, Y.
|
Huang, S.
| +4
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Thema: Case Reports
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337
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Medicine
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World journal of clinical cases
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Journal of the Chinese Medical Association : JCMA
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Chang Gung medical journal
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The Kaohsiung journal of medical sciences
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Acta neurologica Taiwanica
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Frontiers in oncology
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case report
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