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A familial case of Leigh Disease related to NDUFV1 homozygous mutations

European journal of paediatric neurology, 2017-06, Vol.21, p.e133-e134

2017

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DIAPH1 homozygous mutation associated with microcephaly, blindness, and seizures

European journal of paediatric neurology, 2017-06, Vol.21, p.e60-e60

2017

Volltextzugriff (PDF)

PP01.12 – 2602: Differential diagnosis of progressive myoclonic epilepsia: Five patients with Lafora disease

European journal of paediatric neurology, 2015-05, Vol.19, p.S32-S32

2015

Volltextzugriff (PDF)

P176 – 2905: Neurological manifestations and clinical outcomes of Hashimoto thyroiditis in children

European journal of paediatric neurology, 2015-05, Vol.19, p.S143-S143

2015

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P156 – 2357: Torticollis: Different etiologic conditions in childhood

European journal of paediatric neurology, 2015-05, Vol.19, p.S137-S137

2015

Volltextzugriff (PDF)

PP15.8 – 2911: A rare cause of ptosis in four years old girl: Superior mediastinal malignant peripheral nevre sheath tumor

European journal of paediatric neurology, 2015-05, Vol.19, p.S91-S92

2015

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The clinical findings and outcome of 37 patients with tuberous sclerosis

European journal of paediatric neurology, 2008, Vol.12, p.S26-S27

2008

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ETP028 Effects of common anti-epileptic drugs and oxcarbazepine monotherapy on serum levels of homocysteine, vitamin B12, folic acid

European journal of paediatric neurology, 2007, Vol.11, p.121-121

2007

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ETP017 Levetirecetam monotherapy in newly diagnosed cryptogenic West syndrome

European journal of paediatric neurology, 2007, Vol.11, p.86-86

2007

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Guillain–Barré Syndrome Associated with Legionnella Infection

Journal of tropical pediatrics (1980), 2008-08, Vol.54 (4), p.275-277

2008

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CPP013 Late hemorrhagic disease of newborn and neurologic sequelae in Kayseri

European journal of paediatric neurology, 2007, Vol.11, p.48-48

2007

Volltextzugriff (PDF)

IAP011 Primary solitary and multiple hydatid cysts of the brain

European journal of paediatric neurology, 2007, Vol.11, p.58-58

2007

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SP09 Reversible posterior leukoencephalopathy syndrome in childhood: report of nine cases and review of the literature

European journal of paediatric neurology, 2007, Vol.11, p.66-66

2007

Volltextzugriff (PDF)

NOP02 Desmoplastic non-infantile ganglioglioma: case report

European journal of paediatric neurology, 2007, Vol.11, p.117-117

2007

Volltextzugriff (PDF)

MLP013 Bilateral radial and peroneal neuropathy after bariatric surgery in a morbid obese adolescent

European journal of paediatric neurology, 2007, Vol.11, p.70-70

2007

Volltextzugriff (PDF)

An assessment of the relation between vitamin D levels and electroencephalogram (EEG) changes in migraine patients

Bratislavské lékarské listy, 2022, Vol.123 (2), p.92-99

2022

Volltextzugriff (PDF)

Severe Walker–Warburg syndrome associated with new mutation in ISPD gene identified with whole exome sequencing

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S165-S165

2016

Volltextzugriff (PDF)

Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum

Clinical genetics, 2013-10, Vol.84 (4), p.394-395

2013

Volltextzugriff (PDF)

Joubert syndrome: review and report of seven new cases

European journal of neurology, 2004-08, Vol.11 (8), p.505-510

2004

Volltextzugriff (PDF)

Cohen syndrome with acanthosis nigricans and insulin resistance

Journal of pediatric endocrinology & metabolism : JPEM, 2001-06, Vol.14 (6), p.807

2001

Volltextzugriff (PDF)

Lack of serum antineuronal antibodies in children with autism

Bratislavské lékarské listy, 2016, Vol.117 (2), p.77-79

2016

Volltextzugriff (PDF)

Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database

European journal of paediatric neurology, 2017-11, Vol.21 (6), p.864-872

2017

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P174 – 2732: Increased serum phthalates (MEHP, DEHP) and bisphenol A concentrations in children with autism: The role of endocrin disruptors in autism aetiopathogenesis

European journal of paediatric neurology, 2015-05, Vol.19, p.S142-S143

2015

Volltextzugriff (PDF)

Childhood Guillain-Barré syndrome: MR imaging in diagnosis and follow-up

Acta radiologica (1987), 2003-03, Vol.44 (2), p.230-235

2003

Volltextzugriff (PDF)

Serum osteocalcin levels in type I diabetes mellitus

Turkish journal of pediatrics, 1995-10, Vol.37 (4), p.323

1995

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A familial case of Leigh Disease related to NDUFV1 homozygous mutations

DIAPH1 homozygous mutation associated with microcephaly, blindness, and seizures

PP01.12 – 2602: Differential diagnosis of progressive myoclonic epilepsia: Five patients with Lafora disease

P176 – 2905: Neurological manifestations and clinical outcomes of Hashimoto thyroiditis in children

P156 – 2357: Torticollis: Different etiologic conditions in childhood

PP15.8 – 2911: A rare cause of ptosis in four years old girl: Superior mediastinal malignant peripheral nevre sheath tumor

The clinical findings and outcome of 37 patients with tuberous sclerosis

ETP028 Effects of common anti-epileptic drugs and oxcarbazepine monotherapy on serum levels of homocysteine, vitamin B12, folic acid

ETP017 Levetirecetam monotherapy in newly diagnosed cryptogenic West syndrome

Guillain–Barré Syndrome Associated with Legionnella Infection

CPP013 Late hemorrhagic disease of newborn and neurologic sequelae in Kayseri

IAP011 Primary solitary and multiple hydatid cysts of the brain

SP09 Reversible posterior leukoencephalopathy syndrome in childhood: report of nine cases and review of the literature

NOP02 Desmoplastic non-infantile ganglioglioma: case report

MLP013 Bilateral radial and peroneal neuropathy after bariatric surgery in a morbid obese adolescent

An assessment of the relation between vitamin D levels and electroencephalogram (EEG) changes in migraine patients

Severe Walker–Warburg syndrome associated with new mutation in ISPD gene identified with whole exome sequencing

Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum

Joubert syndrome: review and report of seven new cases

Cohen syndrome with acanthosis nigricans and insulin resistance

Lack of serum antineuronal antibodies in children with autism

Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database

P174 – 2732: Increased serum phthalates (MEHP, DEHP) and bisphenol A concentrations in children with autism: The role of endocrin disruptors in autism aetiopathogenesis

Childhood Guillain-Barré syndrome: MR imaging in diagnosis and follow-up

Serum osteocalcin levels in type I diabetes mellitus

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