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Journal Article
Zhonghua Shiyan Yanke Zazhi/Chinese Journal of Experimental Ophthalmology, ISSN 2095-0160, 11/2018, Volume 36, Issue 11, pp. 892 - 896
Journal Article
Nippon Ganka Gakkai zasshi, ISSN 0029-0203, 06/2017, Volume 121, Issue 6, p. 487
Familial exudative vitreoretinopathy is a hereditary insufficiency of retinal vascularture, which manifests a variety of vitreoretinal abnormalities, including... 
Recurrence | Eye Diseases, Hereditary - diagnostic imaging | Retinal Diseases - etiology | Humans | Eye Diseases, Hereditary - therapy | Retinal Diseases - therapy | Eye Diseases, Hereditary - etiology | Financing, Organized | Retinal Diseases - diagnostic imaging
Journal Article
Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, ISSN 1008-9292, 05/2016, Volume 45, Issue 6, p. 636
Hereditary vitreous degeneration muddy is rare in clinic. Here we report ten cases (thirteen eyes) of hereditary vitreous degeneration muddy from two families.... 
Eye Diseases, Hereditary - pathology | Medicine, Chinese Traditional | Humans | Eye Diseases, Hereditary - diagnosis | Male | Eye Diseases, Hereditary - surgery | Retinal Detachment - surgery | Retinal Detachment - diagnosis | Eye Diseases, Hereditary - therapy | Vitreous Body - pathology | Female | Vitrectomy | Vitreous Body - surgery
Journal Article
Klinische Monatsblatter fur Augenheilkunde, 12/2017, Volume 234, Issue 12, p. 1541
Journal Article
Journal Article
Revue medicale suisse, ISSN 1660-9379, 01/2009, Volume 5, Issue 186, p. 118
Recently, preliminary results of three clinical gene therapy trials for early onset retinitis pigmentosa--Leber congenital amaurosis--suggested that treating... 
Genetic Therapy | Humans | Eye Diseases, Hereditary - therapy
Journal Article
Klinische Monatsblatter fur Augenheilkunde, 03/2017, Volume 234, Issue 3, p. 320
Characteristics of inherited retinal dystrophies include deficiencies in light perception and nervous conduction within the retina, leading to reduced vision... 
Gene Transfer Techniques | Animals | Humans | Retinal Dystrophies - therapy | Eye Diseases, Hereditary - therapy | Treatment Outcome | Evidence-Based Medicine | Retinal Dystrophies - genetics | Genetic Vectors - genetics | Eye Diseases, Hereditary - genetics | Genetic Therapy - methods
Journal Article
Klinische Monatsblatter fur Augenheilkunde, 03/2017, Volume 234, Issue 3, p. 329
New genome editing tools in molecular biology are revolutionising precise genome surgery and have greatly influenced experimental ophthalmology too. Aside from... 
Ophthalmology - trends | Animals | Genetic Research | Humans | Eye Diseases, Hereditary - therapy | Gene Editing - methods | Evidence-Based Medicine | Eye Diseases, Hereditary - genetics | Genetic Therapy - methods
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2015, Volume 96, Issue 6, pp. 971 - 978
Heparan and chondroitin/dermatan sulfated proteoglycans have a wide range of roles in cellular and tissue homeostasis including growth factor function,... 
PROTEOGLYCANS | OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME | INITIATION | BIOSYNTHESIS | DISEASE | GENETICS & HEREDITY | DISORDERS | HEPARAN-SULFATE | B3GALT6 | SPECTRUM | XYLOSYLTRANSFERASE-II | Immunohistochemistry | Osteochondrodysplasias - pathology | Retinal Detachment - pathology | Humans | Cataract - pathology | Molecular Sequence Data | Male | Retinal Detachment - drug therapy | Hearing Disorders - genetics | Osteochondrodysplasias - drug therapy | Osteochondrodysplasias - genetics | Base Sequence | Osteoporosis - diagnostic imaging | Diphosphonates - therapeutic use | Craniofacial Abnormalities - pathology | Osteoporosis - genetics | Pentosyltransferases - blood | Real-Time Polymerase Chain Reaction | Craniofacial Abnormalities - genetics | Frameshift Mutation - genetics | Pentosyltransferases - genetics | Eye Diseases, Hereditary - pathology | Craniofacial Abnormalities - drug therapy | Retinal Detachment - genetics | Sequence Analysis, DNA | Eye Diseases, Hereditary - drug therapy | Eye Diseases, Hereditary - genetics | Radiography | Homozygote | Exome - genetics | Pedigree | Hearing Disorders - pathology | Cataract - genetics | Cataract - drug therapy | Genetic disorders | Proteoglycans | Gene mutations | Physiological aspects | Nucleotide sequencing | Identification and classification | Health aspects | Methods | DNA sequencing | Homeostasis | Genotype & phenotype | Genetics | Mutation | RNA-protein interactions | Index Medicus | Report
Journal Article
Klinische Monatsblatter fur Augenheilkunde, 03/2017, Volume 234, Issue 3, p. 272
Journal Article
Journal of Heredity, ISSN 0022-1503, 2003, Volume 94, Issue 1, pp. 31 - 37
Journal Article
Journal of Medical Case Reports, ISSN 1752-1947, 05/2017, Volume 11, Issue 1, pp. 135 - 135
Castleman disease is a rare lymphoproliferative disorder presenting with localized or disseminated lymphadenopathy and systemic manifestations. It can be... 
Hyaline-vascular | Case report | Multiple system involvement | Sri Lanka | Castleman disease | Rituximab | Multicentric | Hepatomegaly - pathology | Intestinal Diseases - complications | Castleman Disease - drug therapy | Vascular Diseases - complications | Skin Abnormalities - complications | Humans | Castleman Disease - diagnosis | Eye Diseases, Hereditary - diagnosis | Lymphadenopathy - etiology | Proteinuria - pathology | Skin Abnormalities - diagnosis | Rituximab - therapeutic use | Adult | Female | Skin Abnormalities - drug therapy | Diarrhea - complications | Vascular Diseases - drug therapy | Proteinuria - etiology | Eye Diseases, Hereditary - complications | Intestinal Diseases - drug therapy | Treatment Outcome | Antihypertensive Agents - therapeutic use | Vascular Diseases - diagnosis | Eye Diseases, Hereditary - drug therapy | Diarrhea - diagnosis | Intestinal Diseases - diagnosis | Lymphadenopathy - pathology | Castleman Disease - complications | Diuretics - therapeutic use | Diarrhea - drug therapy | Sentinel Lymph Node Biopsy | Hepatomegaly - etiology | Immunologic Factors - therapeutic use | Care and treatment | Lymphoproliferative disorders | Diagnosis | Risk factors | Urine | Lymphatic system | Kidneys | Hematology | Laboratories | Cancer therapies | Blood | Proteins | Case studies | Hepatitis | Biopsy | Lymphocytes | Human immunodeficiency virus--HIV | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
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