Topic: Male

Journal: Journal of Child Neurology

Documents

A list of abstracts that contain a topic of "Male" and a journal name of "Journal of Child Neurology".

Mitochondrial Encephalomyopathy Due to a Novel Mutation in the Trnaglu of Mitochondrial Dna.

PMID: 17715279
Unusual Diagnosis in a Child Suffering from Juvenile Alexander Disease: Clinical and Imaging Report.

PMID: 17156703
Focal Cerebral Pathology Presenting As Tonic Seizures.

PMID: 16970894
Case of X-linked Myopathy with Excessive Autophagy.

PMID: 16901453
Evolution of Serum Lipids and Lipoprotein (A) Levels in Epileptic Children Treated with Carbamazepine, Valproic Acid, and Phenobarbital.

PMID: 16551453
Selenoprotein N Muscular Dystrophy: Differential Diagnosis for Early-onset Limited Mobility of the Spine.

PMID: 16900928
Latent and Potential Celiac Disease in Epileptic Turkish Children.

PMID: 16551445
Familial Robertsonian 13;14 Translocation with Mental Retardation and Epilepsy.

PMID: 16948942
Fgfr3 Mutations and Medial Temporal Lobe Dysgenesis.

PMID: 17621485
Epilepsy and Chromosomal Rearrangements in Smith-magenis Syndrome [Del(17)(P11.2p11.2)].

PMID: 16566870
Dignified Death for Severely Impaired Infants: Beyond the Best-interest Standard.

PMID: 17641260
Behavioral Therapy for Treatment of Stereotypic Movements in Nonautistic Children.

PMID: 16566875
Electromyography (Emg) Accuracy Compared to Muscle Biopsy in Childhood.

PMID: 17715269
Cockayne Syndrome in Adults: Review with Clinical and Pathologic Study of a New Case.

PMID: 17092472
Nutritional Vitamin D Deficiency Presenting As Hemichorea.

PMID: 17608310
Efficacy of the Ketogenic Diet As a Treatment Option for Epilepsy: Meta-analysis.

PMID: 16901419
Deep Sedation with Propofol in Patients with Rett Syndrome.

PMID: 17005101
Self-reported Treatment Patterns in Patients with Sturge-weber Syndrome and Migraines.

PMID: 17641257
Muscle Phosphofructokinase Deficiency with Neonatal Seizures and Nonprogressive Course.

PMID: 17608317
Epilepsy in Children in Navarre, Spain: Epileptic Seizure Types and Epileptic Syndromes.

PMID: 17715273

Medical Journals

Topic: Male

Journal: Journal of Child Neurology

Documents

Mitochondrial Encephalomyopathy Due to a Novel Mutation in the Trnaglu of Mitochondrial Dna.

Unusual Diagnosis in a Child Suffering from Juvenile Alexander Disease: Clinical and Imaging Report.

Focal Cerebral Pathology Presenting As Tonic Seizures.

Case of X-linked Myopathy with Excessive Autophagy.

Evolution of Serum Lipids and Lipoprotein (A) Levels in Epileptic Children Treated with Carbamazepine, Valproic Acid, and Phenobarbital.

Selenoprotein N Muscular Dystrophy: Differential Diagnosis for Early-onset Limited Mobility of the Spine.

Latent and Potential Celiac Disease in Epileptic Turkish Children.

Familial Robertsonian 13;14 Translocation with Mental Retardation and Epilepsy.

Fgfr3 Mutations and Medial Temporal Lobe Dysgenesis.

Epilepsy and Chromosomal Rearrangements in Smith-magenis Syndrome [Del(17)(P11.2p11.2)].

Dignified Death for Severely Impaired Infants: Beyond the Best-interest Standard.

Behavioral Therapy for Treatment of Stereotypic Movements in Nonautistic Children.

Electromyography (Emg) Accuracy Compared to Muscle Biopsy in Childhood.

Cockayne Syndrome in Adults: Review with Clinical and Pathologic Study of a New Case.

Nutritional Vitamin D Deficiency Presenting As Hemichorea.

Efficacy of the Ketogenic Diet As a Treatment Option for Epilepsy: Meta-analysis.

Deep Sedation with Propofol in Patients with Rett Syndrome.

Self-reported Treatment Patterns in Patients with Sturge-weber Syndrome and Migraines.

Muscle Phosphofructokinase Deficiency with Neonatal Seizures and Nonprogressive Course.

Epilepsy in Children in Navarre, Spain: Epileptic Seizure Types and Epileptic Syndromes.

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