Disease: Epilepsy occipital calcifications
- A case of adult-onset Sturge-Weber syndrome type III without intracranial calcification, presenting with transient homonymous hemianopia
- A case of epidermal nevus (Jadassohn's phacomatosis) with changes in the nervous system
- A case of Kallmann syndrome with bilateral calcifications at the basal ganglia
- A case of progressive hemifacial and hemispheric atrophy with multiple hemi-intracerebral calcifications presenting with occipital lobe epilepsy
- A case of Sturge-Weber syndrome with severe temper tantrum
- A rare case of dysembryoplastic neuroepithelial tumour in occipital lobe presenting with only headache
- A study of Gobbi's syndrome in Spanish population
- Adult coeliac disease, epilepsy and cerebral calcifications. A case report
- Adult Sturge-Weber syndrome without facial hemangioma: report of one case
- Aluminium in Brain Tissue in Epilepsy: A Case Report from Camelford
- An operated case of intractable occipital lobe epilepsy associated with calcification in the occipital lobe
- Analysis of the concept of the Zika Virus congenital syndrome
- Association between coeliac disease, epilepsy and brain atrophy
- Asymptomatic bilateral occipital calcifications. A possible atypical form of Sturge-Weber-Krabbe syndrome?
- Asymptomatic cerebral calcification--a previously unrecognized feature
- Atypical evolution of benign partial epilepsy in children
- Bilateral occipital calcification associated with celiac disease, folate deficiency, and epilepsy
- Bilateral occipital calcification, epilepsy and coeliac disease: case report
- Bilateral occipital calcification, epilepsy and coeliac disease: clinical and neuroimaging features of a new syndrome
- Bilateral occipital endocranial calcifications: a sign of metabolic damage or of a new syndrome?
- Brain white-matter lesions in celiac disease: a prospective study of 75 diet-treated patients
- Calcified cerebral hydatid cyst
- CEC syndrome--a rare manifestation of coeliac disease
- Celiac disease and epilepsy in pediatric patients
- Celiac disease with occipital calcifications: 2 late cases
- Celiac disease, bilateral occipital calcifications and intractable epilepsy: mechanisms of seizure origin
- Celiac disease, epilepsy and cerebral calcifications
- Cerebral occipital calcifications in celiac disease
- Cerebral Paragonimiasis Presenting with Dementia
- Cerebral venous sinus thrombosis in 2 children with celiac disease
- Clinical characteristics, seizure spread patterns and prognosis of seizures associated with a single small cerebral calcific CT lesion
- Clinical implications of interictal epileptiform discharges in cognitive functioning in CEC syndrome with evolution into epileptic encephalopathy
- Clinical, pathologic and genetic studies on mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
- Clinicopathologic study of intractable epilepsy-related encephalitis
- Coeliac disease and epilepsy
- Coeliac disease, epilepsy and cerebral calcifications
- Coeliac disease, epilepsy, and cerebral calcifications: association with TG6 autoantibodies
- Coeliac disease, epilepsy, and cerebral calcifications. The Italian Working Group on Coeliac Disease and Epilepsy
- Coeliac disease, folic acid deficiency and epilepsy with cerebral calcifications
- Coeliac disease, unilateral occipital calcifications, and drug-resistant epilepsy: successful lesionectomy
- Convulsive disorder in celiac disease
- Cortical vascular abnormalities in the syndrome of celiac disease, epilepsy, bilateral occipital calcifications, and folate deficiency
- De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspring
- Diagnostic dilemma: Sturge-Weber syndrome, without facial nevus
- Dysembryoplastic neuroepithelial tumor (DNET) with pronounced calcinosis
- Dysembryoplastic neuroepithelial tumors: MR appearance
- Early onset bilateral calcifications and epilepsy
- Encephalofacial angiomatosis sparing the occipital lobe and without facial nevus: on the spectrum of Sturge-Weber syndrome variants?
- Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population
- Epilepsy and celiac disease: favorable outcome with a gluten-free diet in a patient refractory to antiepileptic drugs
- Epilepsy in coeliac disease: not just a matter of calcifications
- Epilepsy with bilateral occipital calcifications: Sturge-Weber variant or a different encephalopathy?
- Epilepsy, bi-occipital calcifications and celiac disease
- Epilepsy, cerebral calcifications and celiac disease
- Epilepsy, cerebral calcifications and clinical or subclinical coeliac disease. Course and follow up with gluten-free diet
- Epilepsy, cerebral calcifications and coeliac disease. The importance of an early diagnosis
- Epilepsy, occipital calcifications, and oligosymptomatic celiac disease in childhood
- EPILEPTIC SEIZURES REVEALING STURGE WEBER'S DISEASE IN A TROPICAL ENVIRONMENT: STUDY OF EIGHT CASES
- Familial unilateral and bilateral occipital calcifications and epilepsy
- Focal cortical-subcortical calcifications (FCSCs) and epilepsy in the Indian subcontinent
- Gangliogliomas: clinical, radiological, and histopathological findings in 51 patients
- Gluten sensitivity and epilepsy: a systematic review
- Hippocampal sclerosis in refractory temporal lobe epilepsy is associated with gluten sensitivity
- Histological heterogeneity of dysembryoplastic neuroepithelial tumour: identification and differential diagnosis in a series of 74 cases
- Increased prevalence of silent celiac disease among Greek epileptic children
- Intracranial calcifications--seizures--celiac disease: a case presentation
- Isolated cortical tuber in an infant with genetically confirmed tuberous sclerosis complex 1 presenting with symptomatic West syndrome
- Leptomeningeal angiomatosis accompanied by hair follicle nevus
- Linear intracerebral calcification after depth electrode implantation
- Linear scleroderma en coup de sabre and brain calcification: is there a pathogenic relationship?
- Meningioangiomatosis with Skull Erosion
- Meningo-cortical calcifying angiomatosis and celiac disease
- Neurocysticercosis with hydrocephalus and secondary bilateral hemianopia
- Neuropsychological changes in coeliac disease
- Non-convulsive status epilepticus and audiogenic seizures complicating a patient with asymmetrical epileptic spasms
- Occipital cerebral calcifications and celiac disease: an additional case
- Occipital epilepsies: identification of specific and newly recognized syndromes
- Occipital leptomeningeal angiomatosis without facial angioma. Could it be considered a variant of Sturge-Weber syndrome?
- Occipital lobe seizures related to clinically asymptomatic celiac disease in adulthood
- Parietal and occipital lobe epilepsy: a review
- Partial seizures, cerebral calcifications and celiac disease
- Pharmacoresistant occipital lobe epilepsy with fixation-off sensitivity in a patient with cerebral calcifications: a video/EEG study
- Portal cavernomatous transformation leading to variceal hemorrhage in Sturge-Webber syndrome. A rare, but possible association
- Presentation, Etiology, Outcome, and Differentiation of Visual Semiology of Adult Occipital Epilepsy From Visual Aura of Migraine Headache: A Prospective Study in a Tertiary Care Center in Bangladesh
- Rare Neurological Manifestation of Celiac Disease
- Refractory occipital lobe epilepsy treated by surgery in a child with chronic encephalitis
- Reversible central neural hyperexcitability: an electroencephalographic clue to hypocalcaemia
- Silent celiac disease in patients with childhood localization-related epilepsies
- Sturge Weber-Like Gyral Calcification Seen in Tuberous Sclerosis Complex 1
- Sturge-Weber syndrome accompanied with multiple congenital intracranial lesions
- Sturge-Weber syndrome with late onset hemiplegic migraine-like attacks and progressive unilateral cerebral atrophy
- Sturge-Weber syndrome without facial nevus
- Sturge-Weber syndrome: a review
- Sturge-Weber syndrome: differential diagnosis of neurocysticercosis
- Successful Treatment of Hereditary Folate Malabsorption With Intramuscular Folinic Acid
- Symptomatic occipital lobe epilepsy
- The spectrum of cranial ultrasound and magnetic resonance imaging abnormalities in congenital cytomegalovirus infection
- Transient Periictal Brain Imaging Abnormality in a Saudi Patient with Probable Celiac Disease Epilepsy and Occipital Calcification Syndrome
- Tuberous sclerosis complex coexistent with hippocampal sclerosis
- Visual disturbances representing occipital lobe epilepsy in patients with cerebral calcifications and coeliac disease: a case series