Detalhe da pesquisa
1.
Broadening the clinical spectrum: molecular mechanisms and new phenotypes of ANO3-dystonia.
Brain
; 2023 Dec 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38079528
2.
Maternal Germline Mosaicism of a de Novo TUBB2B Mutation Leads to Complex Cortical Dysplasia in Two Siblings.
Fetal Pediatr Pathol
; 41(1): 155-165, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32281916
3.
Epilepsy in neurofibromatosis type 1: Diffuse cerebral dysfunction?
Epilepsy Behav
; 98(Pt A): 6-9, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31299535
4.
Severe Lactic Acidosis, Wernicke's Encephalopathy, and Wet Beriberi Due to Thiamine Deficiency in a Child With Leukemia.
Klin Padiatr
; 236(3): 193-196, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38096916
5.
Systemic vasculopathy and hypertension in a child: Questions.
Pediatr Nephrol
; 37(1): 113-115, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34633527
6.
Systemic vasculopathy and hypertension in a child: Answers.
Pediatr Nephrol
; 37(1): 117-119, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34633529
7.
A Multicenter Study of Self-Limited Epilepsy With Centrotemporal Spikes: Effectiveness of Antiseizure Medication With Respect to Spike-Wave Index.
Pediatr Neurol
; 152: 79-86, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38237317
8.
Hematopoietic Stem Cell Transplantation for Myelodysplastic Syndrome in a Child With Klinefelter Syndrome.
J Pediatr Hematol Oncol
; 40(1): 81-82, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28902077
9.
Access to Pediatric Neurology Training and Services Worldwide: A Survey by the International Child Neurology Association.
Neurology
; 101(18): 798-808, 2023 10 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37491325
10.
Trends in the choice of antiseizure medications in juvenile myoclonic epilepsy: A retrospective multi-center study from Turkey between 2010 and 2020.
Seizure
; 99: 48-53, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35594744
11.
The effectiveness and tolerability of clobazam in the pediatric population: Adjunctive therapy and monotherapy in a large-cohort multicenter study.
Epilepsy Res
; 184: 106963, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35749975
12.
Absence of exon 17 c.2970-2872delAAT mutation in Turkish NF1 patients with mild phenotype.
Childs Nerv Syst
; 27(12): 2113-6, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21732117
13.
Diffuse Alveolar Damage Correlation with Clinical Diagnosis of Pediatric Acute Respiratory Distress Syndrome.
J Pediatr Intensive Care
; 10(1): 52-57, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33585062
14.
Screening traumatic life events in preschool aged children: cultural adaptation of Child and Adolescent Trauma Screen (CATS) Caregiver-report 3-6 years version.
Turk J Pediatr
; 63(1): 95-101, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33686831
15.
Response to Carbamazepine in a Case of Kleine-Levin Syndrome.
Indian J Pediatr
; 2024 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38637486
16.
Cardiac Manifestation in a Child With Atypical Hemolytic Uremic Syndrome.
Clin Pediatr (Phila)
; : 99228231223656, 2024 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38243652
17.
Double trouble: Duchenne muscular dystrophy and hemophilia.
Pediatr Blood Cancer
; 60(3): 525, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23255221
18.
Autoimmune Epilepsy and/or Limbic Encephalitis Can Lead to Changes in Sleep Spindles.
Noro Psikiyatr Ars
; 55(4): 320-324, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30622387
19.
Trigeminal Neuropathy as an Initial Manifestation in Pediatric-Onset Mixed Connective Tissue Disease.
Turk Arch Pediatr
; 58(6): 660-663, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37563952
20.
Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.
Brain Dev
; 40(6): 458-464, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29544888