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European Journal of Human Genetics, ISSN 1018-4813, 02/2017, Volume 25, Issue 2, pp. 176 - 182
Journal Article
American Journal of Medical Genetics. Part A, ISSN 1552-4825, 2018, Volume 176, Issue 7, pp. 1602 - 1609
Intellectual disability (ID) and global developmental delay are closely related; the latter is reserved for children under the age of 5 years as it is... 
thinning of the corpus callosum | seizures | congenital anomalies | KIF16B | intellectual disability | MENTAL-RETARDATION | HEREDITARY SPASTIC PARAPLEGIA | DYSPLASIA | DEVELOPMENTAL DELAY | LOCUS | KINESIN | NEUROPATHY | CORPUS-CALLOSUM | DISEASE | GENETICS & HEREDITY | MUTATIONS | Genetic research | Genes | Genetic disorders | Phenotypes | Children | Intelligence | Intellectual disabilities
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2013, Volume 8, Issue 1, pp. 83 - 83
Journal Article
NEUROSCIENCES, ISSN 1319-6138, 10/2019, Volume 24, Issue 4, pp. 257 - 263
Objectives: To review the experience of 2 tertiary centers in Saudi Arabia with intracranial hypertension (IH) in the pediatric population. Methods: We... 
OBESITY | GUIDELINES | BARIATRIC SURGERY | PSEUDOTUMOR CEREBRI | DIAGNOSTIC-CRITERIA | PAPILLEDEMA | CLINICAL NEUROLOGY | CHILDREN
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2002, Volume 26, Issue 5, pp. 365 - 368
Migraine equivalents of infancy, childhood, and adolescence are recognized periodic, paroxysmal syndromes without associated headache that are thought to be... 
ABDOMINAL MIGRAINE | CONFUSIONAL MIGRAINE | PEDIATRICS | BENIGN PAROXYSMAL TORTICOLLIS | CHILDHOOD | INFANCY | CLINICAL NEUROLOGY | Humans | Adolescent | Age of Onset | Migraine Disorders - physiopathology | Child, Preschool | Female | Infant | Male | Migraine Disorders - classification | Child | Ambulatory Care | Migraine Disorders - epidemiology
Journal Article
European Journal of Pediatrics, ISSN 0340-6199, 7/2013, Volume 172, Issue 7, pp. 971 - 975
Puberty is the gradual transition period between childhood and adulthood. Many factors may contribute to the onset of puberty. The objective of the study was... 
Saudi Arabia | Pediatrics | Puberty | Medicine & Public Health | Pubic hair | Axillary hair | Menarche age | Breast | ALLERGIES | RISK | SYMPTOMS | ASTHMA | PEDIATRICS | HEALTH | ATOPY | SWIMMING POOL ATTENDANCE | Body Mass Index | Age Factors | Cross-Sectional Studies | Humans | Breast - growth & development | Reference Values | Puberty - physiology | Adolescent | Statistics, Nonparametric | Menarche - physiology | Female | Child | Teenage girls
Journal Article
Pediatric Neurology, ISSN 0887-8994, 01/2018, Volume 78, pp. 35 - 40
Aicardi-Goutières syndrome is a rare genetic neurological disorder with variable clinical manifestations. Molecular detection of specific mutations is required... 
leukodystrophy | calcification | TREX-1 | Aicardi-Goutières syndrome | TREX1 | DISORDERS | PROGRESSIVE FAMILIAL ENCEPHALOPATHY | SAMHD1 | CLINICAL NEUROLOGY | IFIH1 | INTERFERON-ALPHA | METABOLISM | Aicardi-Goutieres syndrome | DISEASE | PEDIATRICS | INFECTION | MUTATIONS | Ribonucleases - genetics | Seizures - genetics | Humans | Atrophy - pathology | Child, Preschool | Infant | Male | Neurodevelopmental Disorders - genetics | Epilepsy - physiopathology | Autoimmune Diseases of the Nervous System - pathology | Epilepsy - etiology | Libya | Saudi Arabia | Autoimmune Diseases of the Nervous System - physiopathology | Seizures - physiopathology | Seizures - pathology | Qatar | Autoimmune Diseases of the Nervous System - genetics | Nervous System Malformations - physiopathology | Epilepsy - genetics | Female | Nervous System Malformations - genetics | Child | Neurodevelopmental Disorders - etiology | Nervous System Malformations - pathology | Neurodevelopmental Disorders - physiopathology | United Arab Emirates | Muscle Spasticity - pathology | Autoimmune Diseases of the Nervous System - complications | White Matter - pathology | Muscle Spasticity - etiology | Nervous System Malformations - complications | Seizures - etiology | Consanguinity | Muscle Spasticity - physiopathology | Epilepsy - pathology | Muscle Spasticity - genetics | Medicine, Experimental | Medical research | Nervous system diseases | Arab countries
Journal Article
Annals of Saudi Medicine, ISSN 0256-4947, 01/2014, Volume 34, Issue 1, pp. 46 - 53
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 12/2002, Volume 17, Issue 12, pp. 901 - 904
The objective of this study was to compare the clinical and electroencephalographic features of two groups of children with benign epilepsy of childhood with... 
PEDIATRICS | CENTROTEMPORAL SPIKES | MRI | CLINICAL NEUROLOGY | CHILDREN | Epilepsy, Rolandic - drug therapy | Humans | Seizures - drug therapy | Anticonvulsants - therapeutic use | Carbamazepine - therapeutic use | Female | Male | Electroencephalography | Retrospective Studies | Epilepsy, Rolandic - physiopathology
Journal Article
Epilepsia open, ISSN 2470-9239, 12/2018, Volume 3, Issue 4, pp. 524 - 527
Early onset epileptic encephalopathy (EOEE) has been used to encompass Ohtahara syndrome (early infantile epileptic encephalopathy [EIEE]), early myoclonic... 
Journal Article
Pediatric Neurology, ISSN 0887-8994, 11/2002, Volume 27, Issue 5, pp. 410 - 411
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2002, Volume 27, Issue 5, pp. 410 - 411
Journal Article
Pediatric Neurology, ISSN 0887-8994, 05/2002, Volume 26, Issue 5, pp. 365 - 368
Journal Article
Pediatric Neurology, ISSN 0887-8994, 11/2002, Volume 27, Issue 5, pp. 410 - 411
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2002, Volume 27, Issue 1, pp. 49 - 52
Journal Article
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