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학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
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연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
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논문 유사도에 따라 DBpia 가 추천하는 논문입니다. 함께 보면 좋을 연관 논문을 확인해보세요!
Vascular Ehlers-Danlos syndrome with distinct histopathologic features
Journal of Pathology and Translational Medicine
2022 .05
신장 경색으로 발현한 혈관형 엘러스-단로스 증후군 1예
대한내과학회지
2022 .08
Resistance to local anesthesia in people with the Ehlers-Danlos Syndromes presenting for dental surgery
Journal of dental anesthesia and pain medicine
2019 .01
[Secondary publication] Sudden Aortic Rupture in Ehlers-Danlos Syndrome Type IV
대한법의학회지
2016 .01
Treatment of the wide open wound in the Ehlers-Danlos syndrome
Archives of craniofacial surgery : ACFS
2019 .01
Right Hemianopsia and Right-Limb Hypesthesia Associated With Vascular Ehlers-Danlos Syndrome and Antiphospholipid Syndrome
Journal of Clinical Neurology
2024 .01
Ehlers-Danlos syndrome VIII with novel C1R variant accompanying white matter changes
Journal of genetic medicine
2019 .01
엘러스-단로스 증후군에 발생한 자발성 신장동맥 박리
영남의대학술지
2016 .01
엘러스-단로스 증후군에 발생한 자발성 신장동맥 박리
Journal of Yeungnam Medical Science
2016 .06
Cutaneous asthenia (Ehlers-Danlos syndrome) in a Korean short-haired cat
Korean Journal of Veterinary Research(대한수의학회지)
2016 .05
Rare Cases of PLOD1-Related Kyphoscoliotic Ehlers-Danlos Syndrome in a Korean Family Identified by Next Generation Sequencing
Journal of Korean Medical Science
2020 .01
Familial Pancreatic Cancer and the Future of Directed Screening
Gut and Liver
2017 .01
Prenatal Diagnosis of an Ascending Aortic Aneurysm Inherited from the Father: A Case Report of Loeys-Dietz Syndrome Type 1
Perinatology
2021 .09
A Case of Familial Cold Autoinflammatory Syndrome with De Novo NLRP3 Mutation
Annals of Dermatology
2021 .01
Vascular compression syndromes: a pictorial review
ULTRASONOGRAPHY
2022 .07
A Case of Familial Spondyloenchondrodysplasia with Immune Dysregulation Masquerading as Moyamoya Syndrome
Journal of Clinical Neurology
2019 .01
Familial aggregation of inflammatory bowel disease in India: prevalence, risks and impact on disease behavior
Intestinal research
2019 .01
The Prevalence of Founder Mutations among Individuals from Families with Familial Pancreatic Cancer Syndrome
Cancer Research and Treatment
2017 .01
The R278I Mutation of PSEN1 in the Familial Alzheimer Disease
Dementia and Neurocognitive Disorders(대한치매학회지)
2020 .01
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