Varsik P, Buranová D, Kollár B, Fedor-Freybergh P.
Case Reports 2006; 27(1-2): 13-15 PubMed PMID: 16648792 Keywords: Acidosis:etiology, Brain Edema:etiology, Child, Preschool, Humans, Hydronephrosis:congenital, Magnetic Resonance Imaging, Male, Metabolic Diseases:complications, Nephrectomy, Reye Syndrome:complications, Stroke:etiology,. Citation: Three years old boy with developmental renal dysplasia was hit as newborn child by attack of cerebral edema with metabolic disturbances .....
Varsik P, Buranová D, Kollár B, Fedor-Freybergh P. Metabolic stroke in three years old boy as the consequence of metabolic derangement. A case report of recidiving Reye's-like syndrome. Neuro Endocrinol Lett. 2006 Apr; 27(1-2): 13-15
Kollár B, Buranová D, Goldenberg Z, Klobucníková K, Varsik P.
Journal Article 2006; 27(1-2): 16-20 PubMed PMID: 16648779 Keywords: Adult, Aged, Aged, 80 and over, Anticonvulsants:therapeutic use, Brain:pathology, Electroencephalography, Female, Humans, Male, Middle Aged, Risk Factors, Secondary Prevention, Seizures:drug therapy, Social Environment,. Citation: Patients experiencing solitary unprovoked epileptic seizure have different risks of recurrence. The possible risk factors include in par.....
Kollár B, Buranová D, Goldenberg Z, Klobucníková K, Varsik P. Solitary epileptic seizure--the risk of recurrence. Neuro Endocrinol Lett. 2006 Apr; 27(1-2): 16-20
Kurca E, Grofik M, Kucera P, Varsik P.
Case Reports 2005; 26(5): 499-502 PubMed PMID: 16264411 Keywords: Adrenal Insufficiency:complications, Adrenocorticotropic Hormone:deficiency, Adult, Autonomic Nervous System:physiopathology, Chromosomes, Human, Pair 12:genetics, Conjunctival Diseases:complications, Electroencephalography, Epilepsy:genetics, Hormone Rep. Citation: Allgrove syndrome is a rare autosomal recessive disease with achalasia, alacrima, adrenocortical insufficiency, autonomic neuropathy and.....
Kurca E, Grofik M, Kucera P, Varsik P. Familial occurrence of adrenocortical insufficiency in two brothers with Allgrove syndrome. A case report of 4A (Allgrove) syndrome with epilepsy and a new AAAS gene mutation. Neuro Endocrinol Lett. 2005 Oct; 26(5): 499-502
Varsik P, Buranová D, Kollár B, Kucera P, Kondás M, Stofko J.
Journal Article 2005; 26(3): 219-224 PubMed PMID: 15990725 Keywords: Adolescent, Adult, Cerebral Cortex, Cerebral Ventricles, Choristoma, Electroencephalography, Epilepsy:epidemiology, Evoked Potentials, Somatosensory, Female, Humans, Hydrocephalus:epidemiology, Incidence, Magnetic Resonance Imaging, Median Nerve:physiolog. CitationOBJECTIVES: Developmental cerebral dysplasias are frequent causes of epilepsy. The early stage of gestation, mainly the period of neural c.....
Varsik P, Buranová D, Kollár B, Kucera P, Kondás M, Stofko J. The quest of cavum septi pellucidi: obscure chance event discovery or the result of some encoded disturbance? Developmental cerebral dysplasias, cavum septi pellucidi and epilepsy: clinical, MRI and electrophysiological study. Neuro Endocrinol Lett. 2005 Jun; 26(3): 219-224
Kucera P, Goldenberg Z, Varsik P, Buranova D, Traubner P.
Clinical Trial 2005; 26(2): 143-147 PubMed PMID: 15855886 Keywords: Adult, Cerebral Cortex:physiology, Diabetes Complications:physiopathology, Diabetes Mellitus, Type 2:complications, Diabetic Neuropathies:diagnosis, Evoked Potentials, Motor:physiology, Evoked Potentials, Somatosensory:physiology, Humans, Middle Aged, Neu. CitationOBJECTIVES: Diabetic neuropathy and autonomic nervous system neuropathy are recognized as the most common clinical pictures of nervous sys.....
Kucera P, Goldenberg Z, Varsik P, Buranova D, Traubner P. Spinal cord lesions in diabetes mellitus. Somatosensory and motor evoked potentials and spinal conduction time in diabetes mellitus. Neuro Endocrinol Lett. 2005 Apr; 26(2): 143-147
Varsik P, Buranová D, Kollár B, Traubner P, Bozek P, Mikulecký M.
Case Reports 2005; 26(1): 7-12 PubMed PMID: 15726012 Keywords: Adolescent, Adult, Anticonvulsants:therapeutic use, Brain:pathology, Child, Electroencephalography, Epilepsies, Myoclonic:complications, Female, Heme:therapeutic use, Humans, Hydroxymethylbilane Synthase:genetics, Male, Porphyria, Acute Intermittent:compl. CitationOBJECTIVES: Myoclonic epilepsy (ME) syndrome is not rare in north-eastern Europe; it is also seen in various forms. Familial occurrence of.....
Varsik P, Buranová D, Kollár B, Traubner P, Bozek P, Mikulecký M. Familial occurrence of myoclonic epilepsy syndrome and acute intermittent porphyria. Neuro Endocrinol Lett. 2005 Feb; 26(1): 7-12