Works matching DE "STURGE-Weber syndrome"
Results: 350
Dusky erythematous plaques over the lower leg associated with bony deformity.
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- 2022
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- Case Study
Cerebrofacial vascular metameric syndrome associated with Moyamoya syndrome: a rare case report.
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- 2022
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- Case Study
AESTHETIC SURGICAL APPROACH FOR STURGE-WEBER SYNDROME AND FACIAL ARTERIOVENOUS TUMORS.
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- Revista Foco (Interdisciplinary Studies Journal), 2024, v. 17, n. 10, p. 1, doi. 10.54751/revistafoco.v17n10-006
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- Article
Farmer with sturge weber syndrme to the leak.
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- European Psychiatry, 2020, v. 63, p. S537
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- Article
Developmental expression of the Sturge-Weber syndrome-associated genetic mutation in Gnaq: a formal test of Happle's paradominant inheritance hypothesis.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad077
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- Article
Postpartum psychosis in Sturge--Weber syndrome: A case report.
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- 2019
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- Case Study
Headache in Sturge-Weber syndrome: A systematic review.
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- Cephalalgia, 2024, v. 44, n. 6, p. 1, doi. 10.1177/03331024241265881
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- Article
Neonate, Infant, Childhood, and Adolescent Epilepsy Syndromes.
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- Neurodiagnostic Journal, 2023, v. 63, n. 1, p. 58, doi. 10.1080/21646821.2023.2172951
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- Article
Multiple angiomas of the external auditory canal in a patient with Sturge-Weber syndrome.
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- ENT: Ear, Nose & Throat Journal, 2007, v. 86, n. 1, p. 15, doi. 10.1177/014556130708600105
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- Article
Low Dose Irradiation for Diffuse Choroidal Hemangioma.
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- Ophthalmic Genetics, 2008, v. 29, n. 4, p. 186, doi. 10.1080/13816810802385467
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- Article
Epilepsy Mechanisms in Neurocutaneous Disorders: Neurofibromatosis Type 1, and Sturge-Weber Syndrome.
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- Frontiers in Neurology, 2017, v. 8, p. 1, doi. 10.3389/fneur.2017.00087
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- Article
Detailed clinical and electrophysiological illustration of a patient with Sturge–Weber syndrome presenting with prolonged transient neurological symptoms.
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- Journal of Neurosciences in Rural Practice, 2018, v. 9, n. 4, p. 608, doi. 10.4103/jnrp.jnrp_11_18
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- Article
Angiomatosis: A Rare Vascular Proliferation of Head and Neck Region.
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- 2015
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- Case Study
Urine vascular biomarkers in Sturge–Weber syndrome.
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- Vascular Medicine, 2013, v. 18, n. 3, p. 122, doi. 10.1177/1358863X13486312
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- Article
Primary Combined Trabeculotomy-Trabeculectomy for Developmental Glaucomas.
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- Journal of Current Glaucoma Practice, 2010, v. 4, n. 2, p. 91
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- Article
Multidisciplinary approach for evaluation of neurocutaneous disorders in children in Sohag University Hospital, Upper Egypt.
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- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 2, p. 149, doi. 10.1016/j.ejmhg.2015.02.003
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- Article
Courtesy Stigma and Social Support: An Exploration of Fathers' Buffering Strategies and Blocking Rationalizations.
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- Health Communication, 2019, v. 34, n. 13, p. 1543, doi. 10.1080/10410236.2018.1504658
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Aunting as a Call to Public Intellectualism: The Roles of (In)Visibility in Health Communication Research and Service.
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- Health Communication, 2017, v. 32, n. 8, p. 1043, doi. 10.1080/10410236.2016.1196516
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DENTAL TREATMENT OF A STURGE-WEBER PATIENT.
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- International Journal of Clinical Dentistry, 2020, v. 13, n. 4, p. 357
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- Article
Sturge-Weber Syndrome: A Case Study.
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- Neonatal Network, 2006, v. 25, n. 2, p. 89, doi. 10.1891/0730-0832.25.2.89
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Clinical and pathologic features of Sturge-Weber syndrome in patients with refractory epilepsy.
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- American Journal of Clinical Pathology, 2024, v. 161, n. 5, p. 469, doi. 10.1093/ajcp/aqad174
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- Article
The Pathogenesis of Port Wine Stain and Sturge Weber Syndrome: Complex Interactions between Genetic Alterations and Aberrant MAPK and PI3K Activation.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 9, p. 2243, doi. 10.3390/ijms20092243
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Sturge-webber syndrome: An uncommon entity.
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- Indian Journal of Medical Research, 2020, v. 152, p. 73, doi. 10.4103/ijmr.IJMR_2091_19
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Ophthalmic manifestations and management of Sturge-Weber syndrome in long-term observation.
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- Ophthalmology Journal (2450-7873), 2022, v. 7, p. 103, doi. 10.5603/OJ.2022.0017
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- Article
Hemispherectomy Outcomes Favorable in Two Reports.
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- Epilepsy Currents, 2003, v. 3, n. 3, p. 103, doi. 10.1046/j.1535-7597.2003.03311.x
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- Article
Sturge-Weber syndrome associated with transient hydrops fetalis.
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- Journal of Obstetrics & Gynaecology, 1994, v. 14, n. 3, p. 162, doi. 10.3109/01443619409004065
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- Article
A rare type of congenital Sturge-Weber Syndrome: presenting with history of perinatal asphyxia.
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- Clinical Case Reports, 2016, v. 4, n. 8, p. 725, doi. 10.1002/ccr3.561
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Deep cerebral vein expansion with metabolic and neurocognitive recovery in Sturge–Weber syndrome.
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- 2018
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- Publication type:
- Case Study
SPONTANEOUS REGRESSION OF PORT-WINE STAIN.
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- European Journal of Pediatric Dermatology, 2022, v. 32, n. 3, p. 165
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- Article
New vascular classification of port-wine stains: improving prediction of Sturge-Weber risk.
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- British Journal of Dermatology, 2014, v. 171, n. 4, p. 861, doi. 10.1111/bjd.13203
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Patterns of vascular birthmarks: questions and clues.
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- British Journal of Dermatology, 2014, v. 171, n. 4, p. 693, doi. 10.1111/bjd.13316
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Sturge-Weber syndrome.
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- 2000
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- Book Review
Periodontal Management of Sturge-Weber Syndrome.
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- Case Reports in Dentistry, 2013, p. 1, doi. 10.1155/2013/517145
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- Article
Basal cell carcinoma arising within port‐wine stain.
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- International Journal of Dermatology, 2022, v. 61, n. 7, p. e269, doi. 10.1111/ijd.15944
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Orofacial Manifestations of Encephalotrigeminal Angiomatosis: A Case Report and Review of Literature.
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- 2017
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- Case Study
Sturge-Weber syndrome.
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- Nursing Children & Young People, 2018, v. 30, n. 4, p. 21, doi. 10.7748/ncyp.30.4.21.s20
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- Article
A Rare Case of Encephalotrigeminal Angiomatosis: A Case Report.
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- 2017
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- Publication type:
- Case Study
Ocular manifestations of Sturge-Weber syndrome: pathogenesis, diagnosis, and management.
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- Clinical Ophthalmology, 2016, v. 10, p. 871, doi. 10.2147/OPTH.S101963
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Sturge-Weber Syndrome: A Review of Pathophysiology, Genetics, Clinical Features, and Current Management Approache [Corrigendum].
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- 2024
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- Correction Notice
Sturge-Weber Syndrome: A Review of Pathophysiology, Genetics, Clinical Features, and Current Management Approache.
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- Application of Clinical Genetics, 2023, v. 16, p. 63, doi. 10.2147/TACG.S363685
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The prevalence and profile of autism in Sturge–Weber syndrome.
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- Journal of Autism & Developmental Disorders, 2022, v. 52, n. 5, p. 1942, doi. 10.1007/s10803-021-05062-0
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- Article
Anesthesia Considerations for the Patient with Sturge-Weber Syndrome.
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- International Student Journal of Nurse Anesthesia, 2020, v. 19, n. 1, p. 12
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- Article
GNA11‐mutated Sturge–Weber syndrome has distinct neurological and dermatological features.
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- European Journal of Neurology, 2022, v. 29, n. 10, p. 3061, doi. 10.1111/ene.15452
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- Article
Bartonelosis: espectro clínico actual de un viejo patógeno.
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- Medicina Interna de Mexico, 2008, v. 24, n. 3, p. 217
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- Article
Man presents with unilateral ocular hypertension.
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- Ocular Surgery News, 2021, v. 39, n. 12, p. 30
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Worsening blurred vision.
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- Ocular Surgery News, 2014, v. 32, n. 19, p. 62
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- Article
Heterocromia de íris: uma revisão das condições que podem afetar a pigmentação iridiana.
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- Revista Brasileira de Oftalmologia, 2021, v. 80, n. 6, p. 1, doi. 10.37039/1982.8551.20210050
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Bilateral Sturge-Weber Syndrome and glaucoma controlled with Ahmed valve implant.
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- Revista Brasileira de Oftalmologia, 2015, v. 74, n. 1, p. 37, doi. 10.5935/0034-7280.20150008
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RASA1 gene alterations in patients with sprodic Sturge -- Weber syndrome.
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- China Journal of Oral & Maxillofacial Surgery, 2010, v. 8, n. 6, p. 482
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- Article
Research advances in pathophysiologic mechanism of Sturge -Weber syndrome.
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- China Journal of Oral & Maxillofacial Surgery, 2009, v. 7, n. 5, p. 470
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- Article