• A case of Sneddon syndrome started with 
neurological symptoms
• A case of Sneddon syndrome started with neurological symptoms
• A case of Sneddon's syndrome associated with Moskowitz's syndrome
• A NOTCH3 homozygous nonsense mutation in familial Sneddon syndrome with pediatric stroke
• A woman with skin lesions and brain infarcts
• Absence of germline mutations in BAP1 in sporadic cases of malignant mesothelioma
• Adenosine Deaminase Two and Immunoglobulin M Accurately Differentiate Adult Sneddon's Syndrome of Unknown Cause
• Advances in Management of the Stroke Etiology One-Percenters
• An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report
• An unusual case of intracerebral hemorrhage: exploring the link with Sneddon's syndrome
• Antiphospholipid antibody positive Sneddon syndrome: a case report
• Antiphospholipid-negative Sneddon's syndrome: A comprehensive overview of a rare entity
• Aortic valve replacement in a patient with Sneddon syndrome
• Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
• Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
• Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia
• BRANCH RETINAL ARTERY OCCLUSION ASSOCIATED WITH PARACENTRAL ACUTE MIDDLE MACULOPATHY IN A PATIENT WITH LIVEDO RETICULARIS
• Cardiac manifestations of Sneddon's syndrome
• Cerebrovascular events, headache and livedoracemosa - diagnosis at a glance?
• Characteristic imaging features of neurovascular involvement in primary Sneddon's syndrome: an analysis of 12 cases
• CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
• Clinical and Histopathologic Characteristics of the Main Causes of Vascular Occusion - Part II: Coagulation Disorders, Emboli, and Other
• Clinically Acquired High Sensitivity Cardiac Troponin T is a Poor Predictor of Reduced Left Ventricular Ejection Fraction After ST Elevation Myocardial Infarction: A National Cohort Study-ANZACS-QI 65
• CME-Dermatologie 11/Auflösung: Blitzfiguren, Atrophie blanche und schmerzhafte Beinulzera
• CNS vasculopathies: Challenging mimickers of primary angiitis of the central nervous system
• Coexistence of scleromyxedema and Sneddon syndrome
• Cognitive and psychiatric changes as first clinical presentation in Sneddon syndrome
• Cognitive and psychiatric signs revealing Sneddon syndrome: A case report
• Combination therapy for Sneddon syndrome to reduce the incidence of cerebrovascular complications
• Concomitant myocardial injury and valvular disease in Sneddon syndrome: a case report
• Cutis marmorata in decompression illness may be cerebrally mediated: a novel hypothesis on the aetiology of cutis marmorata
• Digital ulcers secondary to Sneddon's syndrome successfully treated with Bosentan: not only useful in Systemic Sclerosis
• Echocardiographic features in antiphospholipid-negative Sneddon's syndrome and potential association with severity of neurological symptoms or recurrence of strokes: a longitudinal cohort study
• Extensive giant fusiform aneurysm in Sneddon syndrome
• Freiberg's Infarction as the First Clinical Presentation of Sneddon Syndrome
• Generalized Net-like Erythema and Stroke in a Young Female
• Heritable and non-heritable uncommon causes of stroke
• Hidden in the Rash: A Sneddon Syndrome Case Report
• Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders
• Idiopathic livedo racemosa presenting with splenomegaly and diffuse lymphadenopathy
• Inadequate response to antiplatelet therapy in Sneddon's syndrome. Time to re-evaluate management recommendations?
• Interleukin-17E, inducible nitric oxide synthase and arginase1 as new biomarkers in the identification of neutrophilic dermatoses
• Ischemic stroke in young patients: about 6 cases
• Livedo racemosa generalisata: an anthological vision through Vladímir Lébedev painting
• Livedo racemosa in neurological diseases: an update on the differential diagnoses
• Livedo racemosa: a cutaneous manifestation of Sneddon's syndrome
• Livedo Racemosa: Clinical, Laboratory, and Histopathological Findings in 33 Patients
• Localized livedo racemosa as an indicator for giant cell arteritis
• Long-term follow-up of early-onset Sneddon syndrome: A case report
• Mechanisms of kidney disease in Sneddon's syndrome: Case report and literature review

• Mechanisms of kidney disease in Sneddon's syndrome: Case report and literature review
• Neutrophilic dermatoses
• Non-Hodgkin's lymphoma presenting as Sneddon syndrome
• Non-infective endocarditis
• Not all <em>SCN1A</em> epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype
• Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype
• Novel heterozygous COL4A2 variant c.2572A &gt; G, p.(I858V) mimicking Sneddon's and Divry van Bogaert Syndrome
• Novel heterozygous COL4A2 variant c.2572A > G, p.(I858V) mimicking Sneddon's and Divry van Bogaert Syndrome
• Obstructive valve thrombosis after transcatheter aortic valve replacement (TAVR) in Sneddon syndrome without antiphospholipid antibodies
• Occlusive Nonvasculitic Vasculopathy
• Personality-specific carry-over effects on breeding
• Primary Antiphospholipid Syndrome with Livedo Reticularis is Linked to Female Sex and Stroke and Negatively Associated with Thyroid Disease
• Psychosis with suicide attempt in Sneddon syndrome
• Recurrent stroke, acrocyanosis and livedo racemosa: is it always Sneddon's syndrome?
• Renal involvement in Sneddon syndrome
• Renal involvement in Sneddon's syndrome
• Sneddon syndrome
• Sneddon Syndrome
• Sneddon Syndrome
• Sneddon syndrome and non-bacterial thrombotic endocarditis: a clinicopathological study
• Sneddon syndrome associated with two novel ADA2 gene mutations
• Sneddon syndrome--imaging findings
• Sneddon Syndrome: A Case Report Exploring the Current Challenges Faced with Diagnosis and Management
• Sneddon Syndrome: A Case Report From Saudi Arabia
• Sneddon syndrome: a comprehensive clinical review of 53 patients
• Sneddon Syndrome: A Comprehensive Overview
• Sneddon syndrome: a rare cause of stroke hidden in plain sight
• Sneddon syndrome: anaesthetic and surgical challenges in cardiac valve surgery
• Sneddon syndrome: under diagnosed disease, complex clinical manifestations and challenging diagnosis. A case-based review
• Sneddon-Sydrom: Selten, jedoch wissenswert
• Sneddon's syndrome
• Sneddon's Syndrome and the Capability to Work: With Regard to a Clinical Case
• Sneddon's syndrome concurrent with cerebral venous sinus thrombosis: A case report
• Sneddon's syndrome in a young woman with antiphospholipid syndrome, ischaemic apoplexy and epileptic seizures
• Sneddon's syndrome with optic disc macroaneurysm and macular edema successfully treated with subtenon steroid injection
• Sneddon's Syndrome with Underlying Protein S Deficiency and Decreased Protein C Activity
• Sneddon's syndrome: a comprehensive review of the literature
• Sneddon's syndrome: it is all in the ectoderm
• Stent-graft Repair of a True Internal Thoracic Artery Aneurysm
• Strokes in Sneddon syndrome without antiphospholipid antibodies
• Superficial Siderosis and Microbleed Restricted in Cortex Might Be Correlated to Atrophy and Cognitive Decline in Sneddon's Syndrome
• Teaching NeuroImages: Sneddon syndrome
• The diagnostic challenge of Divry van Bogaert and Sneddon Syndrome: Report of three cases and literature review
• The diagnostic value of skin biopsies in Sneddon syndrome
• The Relevance of Skin Biopsies in General Internal Medicine: Facts and Myths
• Three cases of Sneddon syndrome: A comparison with lymphocytic thrombophilic arteritis
• Treatment of Skin Ulcers Secondary to Sneddon Syndrome With Alprostadil (Prostaglandin E1)
• Triple positive profile in antiphospholipid syndrome: prognosis, relapse and management from a retrospective multicentre study
• Unusual case of retinal arterial branch occlusion: possible variant of Sneddon syndrome
• Vasculopathies, cutaneous necrosis and emergency in dermatology