Physician
Neurology
Dr. Generoso G. Gascon, MD
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Generoso Gascon practices Neurology. He studied medicine at Boston University School of Medicine. Boston University School of Medicine has a rank of 30 in research and a 52 in primary care Dr. Generoso G. Gascon is also a published doctor. He has 72 publication published. The most recent publication is: Biotin-responsive basal ganglia disease: a novel entity.
Publications
- Pinar T. Ozand: Clinician-Scientist Extraordinaire.
- Using Whole-Exome Sequencing to Identify Inherited Causes of Autism.
- Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly.
- Werdnig Hoffman's disease (spinal muscular atrophy type I): A clinical study of 25 Saudi nationals in Al-Khobar.
- Language disorders, convulsive disorder, and electroencephalographic abnormalities. Acquired syndrome in children.
- Rett syndrome: review and discussion of current diagnostic criteria.
- A new patient with alpha-ketoglutaric aciduria and progressive extrapyramidal tract disease.
- 3-Methylglutaconic aciduria: ten new cases with a possible new phenotype.
- Pure word deafness (acquired verbal auditory agnosia) in an Arabic speaking patient.
- Chronic and recurrent headaches in children and adolescents.
- Neurophysiologic correlates of organic acidemias: a survey of 107 patients.
- The clinical spectrum of biotin-treatable encephalopathies in Saudi Arabia.
- Neurologic disorders in Saudi children.
- Glutaric aciduria yype 1: First reported cases in three Saudi patients.
- Vigabatrin in medically resistant epilepsies - A preliminary experience with nine Saudi children.
- Landau-Kleffner syndrome with lateral temporal focal cortical dysplasia and mesial temporal sclerosis: a 30-year follow-up.
- Experience of King Faisal Specialist Hospital and Research Center with Saudi organic acid disorders.
- Maple syrup urine disease: findings on CT and MR scans of the brain in 10 infants.
- Increased density of the thalamus on CT scans in patients with GM2 gangliosidoses.
- Prevalence of different types of lysosomal storage diseases in Saudi Arabia.
- Biopterin-dependent hyperphenylalaninemia due to deficiency of 6-pyruvoyl tetrahydropterin synthase.
- Increased intracranial pressure in Alexander disease: a rare presentation of white-matter disease.
- Phenotypic heterogeneity of spinal muscular atrophy mapping to chromosome 5q11.2-13.3 (SMA 5q).
- The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.
- Central auditory processing and attention deficit disorders.
- Successful treatment of cherry red spot-myoclonus syndrome with 5-hydroxytryptophan.
- Treatment of subacute sclerosing panencephalitis.
- Infantile CNS spongy degeneration--14 cases: clinical update.
- Treatment of subacute sclerosing panencephalitis with alpha interferon.
- Biotin-responsive basal ganglia disease: a novel entity.
- Transient mutism following posterior fossa surgery in children.
- Aspartoacylase deficiency and Canavan disease in Saudi Arabia.
- Familial childhood primary lateral sclerosis with associated gaze paresis.
- Chorea as a presentation of herpes simplex encephalitis relapse.
- Ataxia-ocular motor apraxia syndrome: an investigation of cellular radiosensitivity of patients and their families.
- Unusual presentations of propionic acidemia.
- Cytogenetic investigations in three cell types of a Saudi family with ataxia telangiectasia.
- Malignant hyperphenylalaninemia: CT and MR of the brain.
- 3-Hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) lyase deficiency in Saudi Arabia.
- 4-Hydroxybutyric aciduria.
- 3-Ketothiolase deficiency: a review and four new patients with neurologic symptoms.
- Movement disorders in childhood organic acidurias. Clinical, neuroimaging, and biochemical correlations.
- The efficacy of divalproex sodium in the prophylactic treatment of children with Migraine.
- Ethylmalonic aciduria: an organic acidemia with CNS involvement and vasculopathy.
- Canavan disease: CT and MR imaging of the brain.
- Subacute sclerosing panencephalitis.
- Organic acidurias: a review. Part 1.
- Organic acidurias: a review. Part 2.
- Neurometabolic diseases at a national referral center: five years experience at the King Faisal Specialist Hospital and Research Centre.
- Biochemical heterogeneity of infantile central nervous system spongy degeneration.
- Treatment of inherited neurometabolic diseases: the future.
- Response of 6-pyruvoyl-tetrahydropterin synthase deficiency to tetrahydrobiopterin.
- Functional brain imaging in neuropsychiatric disorders of childhood.
- Riyadh chromosome breakage syndrome: mental retardation with depigmentation of the skin and hair.
- Heterogeneity of carboxypeptidase activity in infantile-onset galactosialidosis.
- GM1 gangliosidosis type 2 in two siblings.
- Intraventricular interferon-alpha stops seizures in Rasmussen's encephalitis: a case report.
- Sanfilippo type D presenting with acquired language disorder but without features of mucopolysaccharidosis.
- Coincident neuraminidase and aspartoacylase deficiency associated with chromosome 9Q paracentric inversion in a Saudi family.
- Congenital muscular dystrophy with abnormal radiographic myelin pattern.
- Saudi variant of multiple sulfatase deficiency.
- Ataxia-oculomotor apraxia syndrome.
- Subacute sclerosing panencephalitis: evaluation with CT and MR.
- Atypical chorioretinitis as an early presentation of subacute sclerosing panencephalitis.
- Combined oral isoprinosine-intraventricular alpha-interferon therapy for subacute sclerosing panencephalitis.
- Persistent preceding focal neurologic deficits in children with chronic Epstein-Barr virus encephalitis.
- Supplementation with omega-3 polyunsaturated fatty acids in the management of recurrent Migraines in adolescents.
- Identifying autism loci and genes by tracing recent shared ancestry.
- Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.
- Transient nonketotic hyperglycinemia and defective serotonin metabolism in a child with neonatal seizures.
- Randomized treatment study of inosiplex versus combined inosiplex and intraventricular interferon-alpha in subacute sclerosing panencephalitis (SSPE): international mu...
Schools
Boston University School Of Medicine
DC General Hospital
Chldns Hospital Med Center
VA Hospital
Procedures Preformed
- EEG (Electroencephalogram)
Conditions Treated
- Convulsions
- Epilepsy
- Essential Tremor
- Migraine
- View All
Doctors Specialties
- Neurology
Accepted Insurances
Education
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Boston Children's Hospital -
Boston University School of Medicine
Hospital
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Massachusetts General Hospital
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