Stiff-Person Syndrome and Graves' Disease: A Pediatric Case Report.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16684397
- By:
- Publication type:
- Article
Works matching IS 2329048X AND DT 2016 AND VI 3
Results: 22
1
2
Pelvic-Spinal Analysis and the Impact of Onabotulinum toxin A Injections on Spinal Balance in one Child With Cerebral Palsy.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16679075
- By:
- Publication type:
- Article
3
Complex Phenotype of a Boy With De Novo 16p13.3-13.2 Interstitial Deletion.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16676153
- By:
- Publication type:
- Article
4
Seizures Related to Hypomagnesemia: A Case Series and Review of the Literature.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16674834
- By:
- Publication type:
- Article
5
Occipital Bony Abnormality and Multiple Strokes in a Pediatric Patient: Case Report and Review of the Current Literature.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16674597
- By:
- Publication type:
- Article
6
Further Validation of the SIGMAR1 c.151+1G>T Mutation as Cause of Distal Hereditary Motor Neuropathy.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16669912
- By:
- Publication type:
- Article
7
Pediatric Hereditary Neuralgic Amyotrophy: Successful Treatment With Intravenous Immunoglobulin and Insights Into SEPT9 Pathogenesis.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16668970
- By:
- Publication type:
- Article
8
Neural Correlates of Reward Processing in Typical and Atypical Development.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16667350
- By:
- Publication type:
- Article
9
De Novo 3q22.3q24 Microdeletion in a Patient With Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome, Dandy-Walker Malformation, and Wisconsin Syndrome.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16666362
- By:
- Publication type:
- Article
10
A Mutation in the Tubulin-Encoding TUBB3 Gene Causes Complex Cortical Malformations and Unilateral Hypohidrosis.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16665758
- By:
- Publication type:
- Article
11
A Video Report of Brain-Lung-Thyroid Syndrome in a Japanese Female With a Novel Frameshift Mutation of the NKX2-1 Gene.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16665012
- By:
- Publication type:
- Article
12
Acute Postviral Encephalopathy: Pathologic and Radiologic Correlation in an Atypical Case.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16658845
- By:
- Publication type:
- Article
13
An Unusual Triad in Pediatric Neurology: A Case Report on Cerebral Palsy, Epilepsy, and Duchenne Muscular Dystrophy.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16642948
- By:
- Publication type:
- Article
14
Assessment of Subclinical Pancreatitis in Epileptic Children With Different Treatment Modalities.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16658364
- By:
- Publication type:
- Article
15
Brain Inflammation in an Infant With Hemimegalencephaly, Escalating Seizures, and Epileptic Encephalopathy.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16633629
- By:
- Publication type:
- Article
16
Encephalopathy and Axonal Neuropathy Associated With Mycoplasma Pneumoniae Infection: Response to Intravenous Immunoglobulin Therapy.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16632140
- By:
- Publication type:
- Article
17
MECP2 Duplications in Symptomatic Females: Report on 3 Patients Showing the Broad Phenotypic Spectrum.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16630673
- By:
- Publication type:
- Article
18
Chromosome 12p Deletion Spanning the GRIN2B Gene Presenting With a Neurodevelopmental Phenotype: A Case Report and Review of Literature.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16629980
- By:
- Publication type:
- Article
19
A De Novo Mutation in MTND6 Causes Generalized Dystonia in 2 Unrelated Children.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X15627937
- By:
- Publication type:
- Article
20
Vein of Galen Aneurysmal Malformation in Neonates Presenting With Congestive Heart Failure.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X15624704
- By:
- Publication type:
- Article
21
Clinical Profile of Pediatric Neurological Disorders: Outpatient Department, Khartoum, Sudan.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X15623548
- By:
- Publication type:
- Article
22
Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis and Guillain-Barre Syndrome in a 16-Month-Old Child.
- Published in:
- Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X15620641
- By:
- Publication type:
- Article