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Journal of the Neurological Sciences, ISSN 0022-510X, 12/2017, Volume 383, pp. 188 - 198
Although misdiagnosis of neuromyelitis optica spectrum disorder (NMOSD) with neuropsychiatric systemic lupus erythematosus (NPSLE) or multiple sclerosis (MS)... 
Immune-mediated neuroinflammatory diseases | Neuropsychiatric systemic lupus erythematosus | Multiple sclerosis | Neuromyelitis optica spectrum disorder | MicroRNAs | CIRCULATING MICRORNAS | CRITERIA | NEUROSCIENCES | CLINICAL NEUROLOGY | BIOMARKERS | PATHOGENESIS | MULTIPLE-SCLEROSIS | NEUROMYELITIS-OPTICA | ROLES | DISABILITY | T-CELLS | BLOOD | Index Medicus
Journal Article
Sexual Development, ISSN 1661-5425, 02/2018, Volume 11, Issue 5-6, pp. I - IV
Journal Article
Child and Adolescent Mental Health, ISSN 1475-357X, 11/2016, Volume 21, Issue 4, pp. 209 - 216
Background: Specific reading disorder (dyslexia) is common in primary school students. Data on prevalence rates in Egypt are needed along with better screening... 
Dyslexia | comorbidity | children | specific reading disability | ADHD | PSYCHIATRY | HYPERACTIVITY | ELEMENTARY-SCHOOL | PREVALENCE | PSYCHOLOGY, CLINICAL | DIFFICULTIES | DISABILITY | ABILITIES | PEDIATRICS | SEX-DIFFERENCES | Elementary school students | Anxiety | Comorbidity | Learning disabled | Attention-deficit hyperactivity disorder | Attention deficit disorder | Reading
Journal Article
Meta Gene, ISSN 2214-5400, 02/2017, Volume 11, pp. 104 - 107
Infantile convulsions and choreoathetosis (ICCA) syndrome is a rare neurological genetic disorder inherited in an autosomal dominant manner with incomplete... 
Mutation | Infantile seizure | Paroxysmal choreoathetosis | PRRT2 gene
Journal Article
Comparative Clinical Pathology, ISSN 1618-5641, 7/2013, Volume 22, Issue 4, pp. 741 - 745
Hypertension (HTN) is a chronic condition of concern due to its role in the causation of coronary artery disease (CAD), stroke, and other vascular... 
Pathology | Essential hypertension | Medicine & Public Health | Hematology | Genotyping | Apolipoprotein E | Oncology | Molecular | Hypertension | Analysis | Low density lipoproteins | Genes | Genetic aspects | Triglycerides | Blood lipids | Coronary heart disease | Cholesterol
Journal Article
Sexual Development, ISSN 1661-5425, 02/2018, Volume 11, Issue 5-6, pp. 280 - 283
WT1 gene mutations have been described in 46,XY patients with ambiguous genitalia or complete gonadal dysgenesis with or without Wilms' tumor, nephropathy,... 
Short Report | Gonadoblastoma | 46,XY DSD | Denys-Drash syndrome | Wilms' tumor | Ambiguous genitalia | TUMOR SUPPRESSOR GENE | GENOTYPE/PHENOTYPE CORRELATIONS | DISEASES | SEQUENCE | DEVELOPMENTAL BIOLOGY | EXPRESSION | DENYS-DRASH-SYNDROME | Medical research | Gene mutations | Germ cell tumors | Medicine, Experimental | Genetic aspects | Reproductive organs | Kidney diseases
Journal Article