• KOL
    • Dravet Syndrome
    • Nur Aydınli̇
    • Nur Aydınli̇: Influence Statistics

      Nur Aydınli̇

      Nur Aydınli̇

      Division of Pediatric Neurology, Department of Pediatrics, İstanbul University Faculty of Medicine, İstanbul, Turkey. | Pediatric Genetics, Department of Pediatrics, Acibadem ...

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      Nur Aydınli̇:Expert Impact

      Concepts for whichNur Aydınli̇has direct influence:Dravet syndrome,Infantile spasms,Centrotemporal spikes,West syndrome,Status epilepticus,Antiepileptic drugs,Periventricular leukomalacia,Developmental delay.

      Nur Aydınli̇:KOL impact

      Concepts related to the work of other authors for whichfor which Nur Aydınli̇ has influence:Neonatal seizures,Infantile spasms,Congenital muscular torticollis,Brachial plexus,Antiepileptic drugs,Cerebral palsy,Intracranial hemorrhage.

      KOL Resume for Nur Aydınli̇

      Year
      2020

      Division of Pediatric Neurology, Department of Pediatrics, İstanbul University Faculty of Medicine, İstanbul, Turkey.

      Pediatric Genetics, Department of Pediatrics, Acibadem Mehmet Ali Aydinlar University, Istanbul, Turkey

      2019

      Istanbul Faculty of Medicine, Pediatric Neurology Section, Istanbul University, Istanbul, Turkey

      2018

      Division of Pediatric Neurology, Department of Pediatrics, Istanbul Medical Faculty, Istanbul, Turkey

      2017

      Division of Pediatric Neurology, Department of Pediatrics, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey

      2016

      Division of Pediatric Neurology, Department of Pediatrics, Istanbul University Faculty of Medicine, Istanbul, Turkey

      2015

      Department of Pediatric Neurology, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.

      2014

      Department of Pediatric Neurology, Istanbul Medical Faculty, Istanbul University, Capa, Istanbul, Turkey

      2013

      Department of Pediatric Neurology, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey

      2012

      Department of Pediatric Neurology, Istanbul University, Arpaemini/Fatih, İstanbul 34093, Turkey

      2011

      Pediatric Neurology Unit, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey

      2008

      1Department of Pediatrics, Faculty of Medicine, Eskisehir Osmangazi University, Eskis¸ehir and Departments of 2Pediatric Emergency Service and 3Pediatric Neurology, Medical Faculty of Istanbul, University of Istanbul, Istanbul, Turkey

      2006

      Department of Pediatrics, Division of Pediatric Neurology, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey

      2005

      Division of Child Neurology Department of Pediatrics Istanbul Medical Faculty Istanbul University Istanbul, Turkey

      2004

      Department of Pediatrics, Division of Pediatric Neurology, Istanbul, Turkey

      2003

      Division of Paediatric Neurology, Department of Paediatrics, İstanbul University İstanbul Medical Faculty, Çapa 34390, Istanbul, Turkey

      2000

      Department of Pediatrics, Division of Pediatric Neurology Istanbul University; Istanbul Medical Faculty, Istanbul, Turkey

      1999

      Department of Pediatrics; Division of Pediatric Neurology, Istanbul University, Medical Faculty of Istanbul; Istanbul; Turkey

      1998

      Department of Pediatrics, Istanbul University Faculty of Medicine, Capa.

      Division of Pediatric Neurology; İstanbul Faculty of Medicine; Istanbul, Turkey

      1996

      Division of Pediatric Neurology, Department of Pediatrics, Faculty of Medicine, Istanbul University, Capa 34390, Istanbul, Turkey

      Sample of concepts for which Nur Aydınli̇ is among the top experts in the world.
      Concept World rank
      22 hemorrhagic strokes #2
      365 237 months #2
      hemiplegia chickenpox #3
      79 stroke patients #4
      stroke istanbul #5
      stiripentol seizure frequency #5
      istanbul medical faculty #7
      epilepticus developmental #7
      medicine epileptic #12
      hypohidrosis hyperthermia #16
      seizures rufinamide #17
      dravet syndrome stiripentol #17
      status epilepticus 95 #20
      dre epilepsy electroencephalography #22
      infant epilepsy #22
      lissencephaly brain #26
      longitudinal 25ohd #27
      etiologic yield #29
      floppy infants #30
      pachygyria lissencephaly #32
      thyroid function alterations #33
      congenital brachial #34
      79 stroke #39
      meningeal syndrome #42
      aims correlation #49
      outcome 79 #49
      persistent neurologic deficit #53
      sma pme #53
      onset intracranial #55
      factors dre #56
      passive neck #57
      etiologic evaluation #60
      stroke turkey #66
      stiripentol treatment #68
      smapme #71
      congenital torticollis #72
      panencephalitis presenting #73
      seizures spasm #94
      poor sucking #97
      localizationrelated epilepsies #98

      Prominent publications by Nur Aydınli̇

      KOL-Index: 7390

      Dravet syndrome is a rare and progressive epileptic encephalopathy of infancy. Stiripentol reduces the seizure frequency in patients with Dravet syndrome. We evaluated the clinical characteristics of patients with Dravet syndrome and their response to stiripentol. We retrospectively collected the data of 21 patients (11 females; mean age, 8.2 years, range: 5.4-15 years) with Dravet syndrome who were treated with stiripentol in our outpatient clinic between June 2016 and June 2017. ...

      Known for Dravet Syndrome | Status Epilepticus | Stiripentol Treatment | Seizure Frequency | Epilepsies Myoclonic
      KOL-Index: 6712

      The purpose of this study was to evaluate positron emission tomography (PET) findings in patients diagnosed with infantile spasms and autism. This study includes 90 patients who were diagnosed with infantile spasms at the Department of Pediatric Neurology in the Istanbul University Medical Faculty between 1995 and 2007. Of the 90 patients, 15 patients who were diagnosed with autism using the Autism Behaviour Checklist and Childhood Autism Rating Scale and a control group of nine patients ...

      Known for Infantile Spasms | Emission Tomography | Frontal Lobe | 2 Years | Autism Study
      KOL-Index: 5834

      Population-based studies report that children with epilepsy have relatively better prognosis than those with an onset at infancy, though studies about this period are limited. We aimed to evaluate the etiology in infant epilepsy less than 2 years of age and foreseeable risk factors for anti-epileptic drug resistance. We evaluated the patients who were presented to the division of pediatric neurology in our university hospital with seizures when they were between 1 and 24 months of age ...

      Known for Resistant Epilepsy | Tertiary Center | Status Epilepticus | Developmental Delay | Factors Drug
      KOL-Index: 5764

      Spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME), a rare disorder caused by mutation in the ASAH1 gene, is characterized by progressive muscle weakness and intractable epilepsy. The literature about SMA-PME is very rare and most of the time limited to case reports. Mutation in the ASAH1 gene is also found in another rare syndrome which is Farber disease. We report a case of a 13.5-year-old girl with SMA-PME associated with ASAH1 gene mutation. She presented with ...

      Known for Spinal Muscular Atrophy | Progressive Myoclonic Epilepsy | Farber Disease | Asah1 Gene | Sma Pme
      KOL-Index: 5509

      Thirteen infants with congenital brachial plexus palsy (eight with upper, five with upper and lower) were monitored by magnetic resonance imaging (the first performed between 7 and 41 days of age and the second at 3 months of age), electromyography (the first performed between 27 and 50 days and the second at 3 months), and the muscle scoring system of the Hospital for Sick Children (at 3, 6, and 9 months of age). The findings were evaluated with respect to the clinical status of the ...

      Known for Brachial Plexus | 3 Months | Root Avulsion | Resonance Imaging | Sick Children
      KOL-Index: 4928

      The aim of this study was to evaluate the thyroid function alterations in a group of epileptic children taking antiepileptic drugs (AEDs). Patients demographic data and the free throxine (fT4) and thyroid-stimulating hormone (TSH) levels at the beginning of the treatment and at the third, sixth and ninth months of AED treatment were recorded retrospectively. A total of 106 children, 59 males and 47 females, were enrolled in the study. Mean patient age was 3.7 years, ranging between 3 ...

      Known for Thyroid Hormones | Antiepileptic Therapy | Epileptic Children | Valproic Acid | Tsh Levels
      KOL-Index: 4893

      Bi-allelic loss-of-function variants in genes that encode subunits of the adaptor protein complex 4 (AP-4) lead to prototypical yet poorly understood forms of childhood-onset and complex hereditary spastic paraplegia: SPG47 (AP4B1), SPG50 (AP4M1), SPG51 (AP4E1) and SPG52 (AP4S1). Here, we report a detailed cross-sectional analysis of clinical, imaging and molecular data of 156 patients from 101 families. Enrolled patients were of diverse ethnic backgrounds and covered a wide age range ...

      Known for Spastic Paraplegia | Adaptor Protein | Complex 4 | Corpus Callosum | Clinical Molecular
      KOL-Index: 4218

      This study evaluated etiologic and risk factors affecting long-term prognoses of neurologic outcomes in newborns with neonatal seizures. We enrolled patients at chronologic ages of 23-44 months, referred to the Department of Pediatric Neurology, Istanbul Medical Faculty, from January 1, 2007-December 31, 2009, after manifesting seizures in their first postnatal 28 days. Of 112 newborns, 41 were female, 71 were male, 33 were preterm, and 79 were full-term. Perinatal asphyxia (28.6%) and ...

      Known for Neonatal Seizures | Neurologic Outcomes | Developmental Delay | Gestational Age | Apgar Score
      KOL-Index: 4166

      Floppiness in an infant may have a number of different etiologies from disorders of the brain to spinal cord lesions, neuropathies, neuromuscular junction disorders and myopathies. In this study we aimed to investigate the correlation of muscle ultrasonography (US) and electromyography (EMG) in the diagnosis of floppy infants. The study encompassed 41 floppy infants aged 2-24 months. The muscle US and EMG examinations were performed without awareness of the clinical diagnosis. The final ...

      Known for Muscle Ultrasonography | Floppy Infants | Central Hypotonia | Spinal Muscular | Diagnosis Differential
      KOL-Index: 4096

      Our objective was to characterize the etiologic factors and outcome for stroke in children. We retrospectively reviewed the charts of patients between the ages of 40 days and 94 months (36.5 +/- 23.7 months) with stroke seen at Istanbul Medical Faculty, Department of Pediatrics between January 1995 and December 2003. We found 79 cases of stroke: 57 ischemic and 22 hemorrhagic strokes. Seventeen children had vitamin K deficiency dependent hemorrhage. In 14 children stroke occurred as a ...

      Known for Stroke Children | Factor Leiden | Cardiac Disease | Infant Male
      KOL-Index: 3971

      A retrospective study is presented of the clinical features and outcome of late onset haemorrhagic disease due to vitamin K deficiency in 11 babies who were admitted to the emergency or child neurology unit during a 4-year period (January 1994-December 1997). The disease occurred in infants between 30 and 119 days of age (mean: 56+/-24 days). None of them received vitamin K after birth and all were breastfed. The presenting complaints were seizures (91%), drowsiness (82%), poor sucking ...

      Known for Intracranial Haemorrhage | Late Onset | Vitamin Deficiency | Poor Sucking | Retrospective Studies
      KOL-Index: 3827

      Cranial computed tomography (CT) or magnetic resonance imaging (MRI), or both, of 143 patients with West syndrome were retrospectively reviewed. Twenty-four children had normal CT scans. The most striking findings on pathologic scans were cerebral atrophy, ventricular enlargement, and encephalomalacia. Of 78 children who underwent MRI, 14 had normal scans. Cerebral malformations, cerebral atrophy, and delayed myelination were the most common pathologic findings and were observed in 25, ...

      Known for West Syndrome | Cerebral Atrophy | Delayed Myelination | Infantile Tomography | Imaging Mri
      KOL-Index: 3784

      OBJECTIVE: Developmental delay is a common pediatric problem, having a great number of underlying causal factors. Etiologic diagnosis is important for providing information about pathogenesis, prognosis, recurrence risk and specific medical interventions. The aim of this study was to determine the etiologic yield and spectrum of a consecutive cohort of global developmentally delayed children.

      METHODS: This retrospective study included all children younger than 5 years of age with global ...

      Known for Developmental Delay | Etiologic Diagnosis | Physical Examination | Initial Evaluation | Children Global
      KOL-Index: 3760

      Antiepileptic drugs (AED) have potential side effects through vitamin-D. Prevalence of vitamin D insufficiency and potential risk factors for the longitudinal changes of vitamin D levels compared to its baseline levels under AED treatment were investigated in this study. This retrospective study includes patients whose AED therapy were started in only autumn months, between 2000 and 2014. Detailed assessment of neurologic diagnosis and brain MRI findings, ambulatory status, types and ...

      Known for Antiepileptic Drugs | Vitamin Levels | Potential Risk Factors | Longitudinal 25ohd | Alkaline Phosphatase

      Key People For Dravet Syndrome

      Top KOLs in the world
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      #2
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      #5
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      Division of Pediatric Neurology, Department of Pediatrics, İstanbul University Faculty of Medicine, İstanbul, Turkey. | Pediatric Genetics, Department of Pediatrics, Acibadem Mehmet Ali Aydinlar University, Istanbul, Turkey | Istanbul Faculty of Medi

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