Published in Childs Nerv Syst on October 25, 2005
Cortical abnormalities in epilepsy revealed by local EEG synchrony. Neuroimage (2007) 1.37
A significant proportion of children with morphea en coup de sabre and Parry-Romberg syndrome have neuroimaging findings. Pediatr Dermatol (2012) 1.17
Progressive hemifacial atrophy: a review. Orphanet J Rare Dis (2015) 1.09
Parry-Romberg syndrome: clinical, electrophysiological and neuroimaging correlations. Neurol Sci (2011) 0.97
Neurological Manifestations in Parry-Romberg Syndrome: 2 Case Reports. Medicine (Baltimore) (2015) 0.87
Neurologic involvement in scleroderma en coup de sabre. Autoimmune Dis (2012) 0.87
Scleroderma linearis: hemiatrophia faciei progressiva (Parry-Romberg syndrom) without any changes in CNS and linear scleroderma "en coup de sabre" with CNS tumor. BMC Neurol (2009) 0.87
Overlap between linear scleroderma, progressive facial hemiatrophy and immune-inflammatory encephalitis in a paediatric cohort. Eur J Pediatr (2015) 0.82
Parry Romberg syndrome with a wide range of ocular manifestations: a case report. BMC Ophthalmol (2015) 0.79
CNS imaging findings associated with Parry-Romberg syndrome and en coup de sabre: correlation to dermatologic and neurologic abnormalities. Neuroradiology (2014) 0.79
Chronologic presentation of a severe case of progressive hemifacial atrophy (parry-romberg syndrome) with the loss of an eye. Case Rep Otolaryngol (2014) 0.77
Oral manifestations of Parry-Romberg syndrome: A review of literature. Avicenna J Med (2015) 0.75
Longstanding epileptic encephalopathy and linear localized scleroderma: two distinct pathologic processes in an adolescent. Rheumatol Int (2008) 0.75
Parry-Romberg syndrome: a global survey of 205 patients using the Internet. Neurology (2003) 2.28
Cranial neural crest and the building of the vertebrate head. Nat Rev Neurosci (2003) 2.11
Localized scleroderma in adults and children. Clinical and laboratory investigations on 239 cases. Eur J Dermatol (2003) 2.01
Clinical and radiologic findings in progressive facial hemiatrophy (Parry-Romberg syndrome). AJNR Am J Neuroradiol (1997) 1.68
Scleroderma 'en coup de sabre' and progressive facial hemiatrophy. Is it possible to differentiate them? J Eur Acad Dermatol Venereol (2002) 1.54
Rasmussen's encephalitis: early characteristics allow diagnosis. Neurology (2003) 1.29
The pathology of Rasmussen syndrome: stages of cortical involvement and neuropathological studies in 45 hemispherectomies. Epilepsia (2004) 1.29
Scleroderma "en coup de sabre": pathological evidence of intracerebral inflammation. J Neurol Neurosurg Psychiatry (2001) 1.29
Progressive facial hemiatrophy: central nervous system involvement and relationship with scleroderma en coup de sabre. J Rheumatol (2003) 1.14
Double pathology in Rasmussen's syndrome: a window on the etiology? Neurology (1998) 1.14
Parry-Romberg syndrome with migraine and intracranial aneurysm. Neurology (2002) 1.08
Rasmussen syndrome: multifocal spread of inflammation suggested from MRI and PET findings. Epilepsia (2003) 1.08
Bilateral linear scleroderma "en coup de sabre" associated with facial atrophy and neurological complications. BMC Dermatol (2001) 0.98
Neuropathological findings in a patient with epilepsy and the Parry-Romberg syndrome. Epilepsia (2001) 0.97
Spontaneous carotid-jugular fistula and carotid dissection in a patient with multiple intracranial arachnoid cysts and hemifacial atrophy: a generalized connective tissue disorder? Case report. J Neurosurg (1995) 0.96
MR of brain involvement in progressive facial hemiatrophy (Romberg disease): reconsideration of a syndrome. AJNR Am J Neuroradiol (1994) 0.96
Progressive facial hemiatrophy: abnormality of intracranial vasculature. Neurology (1998) 0.95
Linear scleroderma associated with progressive brain atrophy. Brain Dev (2003) 0.93
Intracranial findings in progressive facial hemiatrophy. J Rheumatol (1992) 0.89
Scleroderma en coup de sabre with central nervous system and ophthalmologic involvement: treatment of ocular symptoms with interferon gamma. J Am Acad Dermatol (2003) 0.89
Rasmussen encephalitis associated with Parry-Romberg syndrome. Neurology (2003) 0.86
Parry-Romberg syndrome: follow-up imaging during suppressive therapy. Neuroradiology (1997) 0.86
Scleroderma-like disorders. Semin Cutan Med Surg (1998) 0.86
Progressive facial hemiatrophy with multiple benign tumors and hamartomas. Neuropediatrics (1995) 0.85
Localized scleroderma: imaging features. Pediatr Radiol (1994) 0.84
Progressive facial hemiatrophy after epileptic seizures. Pediatr Neurol (2000) 0.84
Intracerebral involvement in scleroderma en coup de sabre: report of a case with neuropathologic findings. Ann Neurol (1995) 0.84
Bilateral Rasmussen encephalitis: postmortem documentation in a five-year-old. Epilepsia (2003) 0.83
Progressive facial hemiatrophy and epilepsy: a common underlying dysgenetic mechanism. Neurology (1997) 0.83
Congenital abnormalities of the central nervous system. J Neurol Neurosurg Psychiatry (2003) 0.82
Asymmetry: molecular, biologic, embryopathic, and clinical perspectives. Am J Med Genet (2001) 0.81
Progressive inflammatory lesions of the brain parenchyma in localized scleroderma of the head. J Neurol (1990) 0.80
Scleroderma en coup de sabre with central nervous system involvement. J Dermatol (2000) 0.79
Rasmussen encephalitis. Arch Neurol (2004) 0.75
Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing. Hum Mol Genet (2012) 1.90
CNS-PNETs with C19MC amplification and/or LIN28 expression comprise a distinct histogenetic diagnostic and therapeutic entity. Acta Neuropathol (2014) 1.28
Prevention and management of painful neuroma. Neurol Med Chir (Tokyo) (2006) 1.14
Malignant transformation in the course of a dentigerous cyst: a problem for a clinician and a pathologist. Considerations based on a case report. Pol J Pathol (2013) 1.03
Hereditary neuropathy with liability to pressure palsy. Folia Neuropathol (2006) 0.94
Huntington disease in a 9-year-old boy: clinical course and neuropathologic examination. J Child Neurol (2006) 0.92
Aneurysmal bone cyst of the orbit. Pediatr Neurosurg (2006) 0.91
Randomized clinical trial of prevention of hydrocephalus after intraventricular hemorrhage in preterm infants: brain-washing versus tapping fluid. Pediatrics (2007) 0.90
Isolated rhomboencephalosynapsis - a rare cerebellar anomaly. Pol J Radiol (2012) 0.90
Investigations of differences in iron oxidation state inside single neurons from substantia nigra of Parkinson's disease and control patients using the micro-XANES technique. J Biol Inorg Chem (2006) 0.89
[Schizencephaly--clinical and radiological presentation of pediatric patients]. Wiad Lek (2006) 0.88
Cutting edge issues in the Churg-Strauss syndrome. Clin Rev Allergy Immunol (2013) 0.87
Randomized trial of drainage, irrigation and fibrinolytic therapy for premature infants with posthemorrhagic ventricular dilatation: developmental outcome at 2 years. Pediatrics (2010) 0.87
A novel PANK2 gene mutation: clinical and molecular characteristics of patients short communication. J Child Neurol (2007) 0.85
Morphological aspects of the traumatic chronic subdural hematoma capsule: SEM studies. Microsc Microanal (2007) 0.85
Fetus in fetu: a medical curiosity--considerations based upon an intracranially located case. Childs Nerv Syst (2013) 0.83
Practical approach to childhood craniopharyngioma: a role of an endocrinologist and a general paediatrician. Childs Nerv Syst (2009) 0.83
Expression of tuberin and hamartin in tuberous sclerosis complex-associated and sporadic cortical dysplasia of Taylor's balloon cell type. Folia Neuropathol (2008) 0.83
The T allele of the 677C>T polymorphism of methylenetetrahydrofolate reductase gene is associated with an increased risk of ischemic stroke in Polish children. J Child Neurol (2009) 0.82
Tumours and tumour-like lesions of the spinal canal and spine. A review of 185 consecutive cases with more detailed close-up on some chosen pathologies. Pol J Pathol (2011) 0.82
Does apoptosis occur in amyotrophic lateral sclerosis? TUNEL experience from human amyotrophic lateral sclerosis (ALS) tissues. Folia Neuropathol (2005) 0.81
Biomolecular investigation of human substantia nigra in Parkinson's disease by synchrotron radiation Fourier transform infrared microspectroscopy. Arch Biochem Biophys (2007) 0.81
The natural history of SCO2 deficiency in 36 Polish children confirmed the genotype-phenotype correlation. Mitochondrion (2013) 0.81
[A case of GH and TSH secreting pituitary macroadenoma]. Przegl Lek (2006) 0.81
The cerebral form of toxocarosis in a seven-year-old patient. Folia Neuropathol (2006) 0.81
Melatonin and childhood refractory epilepsy--a pilot study. Med Sci Monit (2010) 0.81
Study of Cu chemical state inside single neurons from Parkinson's disease and control substantia nigra using the micro-XANES technique. J Trace Elem Med Biol (2008) 0.81
Radiological findings in relation to the neurodevelopmental outcome in hydrocephalic children treated with shunt insertion or endoscopic third ventriculostomy. Childs Nerv Syst (2013) 0.79
Friedreich's ataxia. J Child Neurol (2002) 0.79
Paraganglioma of the cauda equina presenting with erectile and sphincter dysfunction. J Chin Med Assoc (2009) 0.78
An integrated experimental and analytical approach to the chemical state imaging of iron in brain gliomas using X-ray absorption near edge structure spectroscopy. Anal Chim Acta (2011) 0.78
Visualisation of the extent of damage in a rat spinal cord injury model using MR microsopy of the water diffusion tensor. Acta Neurobiol Exp (Wars) (2005) 0.77
Congenital subependymal giant cell astrocytomas in patients with tuberous sclerosis complex. Childs Nerv Syst (2014) 0.77
Pituitary enlargement in patients with PROP1 gene inactivating mutation represents cystic hyperplasia of the intermediate pituitary lobe. Histopathology and over 10 years follow-up of two patients. J Pediatr Endocrinol Metab (2009) 0.77
[Myelosis funicularis as a result of secondary vitamin B12 deficiency in a 9-year-old girl]. Wiad Lek (2002) 0.77
Evaluation of quality of life and clinical status of children operated on for intractable epilepsy. Childs Nerv Syst (2006) 0.77
Posterior fossa brain tissue injury: developmental, neuropsychological, and neurological consequences of brain tumors in children. Acta Neurochir Suppl (2010) 0.77
Growth hormone deficiency associated with moyamoya disease in a 16 year-old boy. Hormones (Athens) (2006) 0.77
Increased synphilin-1 expression in human elderly brains with substantia nigra Marinesco bodies. Pharmacol Rep (2009) 0.77
Neuropathological diagnosis of tumour and bridge card game: some personal remarks and considerations (Letter to the Editor). Folia Neuropathol (2005) 0.76
[Congenital brain tumor in neonate--case report and review of literature]. Przegl Lek (2005) 0.76
[Joubert syndrome and related disorders]. Neurol Neurochir Pol (2012) 0.76
Papillary pineocytoma in child: a case report. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub (2007) 0.76
Angelman syndrome revisited. Neurologist (2007) 0.76
Carbohydrate-lipid profile and use of metformin with micronized fenofibrate in reducing metabolic consequences of craniopharyngioma treatment in children: single institution experience. J Pediatr Endocrinol Metab (2015) 0.76
The oxidation states and chemical environments of iron and zinc as potential indicators of brain tumour malignancy grade - preliminary results. Metallomics (2013) 0.76
Elemental micro-imaging and quantification of human substantia nigra using synchrotron radiation based x-ray fluorescence--in relation to Parkinson's disease. J Phys Condens Matter (2012) 0.76
[Endoscopic ventriculostomy of the third ventricle in adults. Own experience]. Neurol Neurochir Pol (2002) 0.76
Classification of nerve cells from substantia nigra of patients with Parkinson's disease and amyotrophic lateral sclerosis with the use of X-ray fluorescence microscopy and multivariate methods. Anal Chem (2005) 0.75
Expression of cyclooxygenase-2 (COX-2) in pituitary tumours. Med Sci Monit (2012) 0.75
Torticollis as a first sign of posterior fossa and cervical spinal cord tumors in children. Childs Nerv Syst (2013) 0.75
[Usefulness of the "P.N." frame in biopsies and stereotactic operations on the brain]. Przegl Lek (2004) 0.75
Clinical and neuropathological picture of familial encephalopathy with bifunctional protein deficiency. Folia Neuropathol (2007) 0.75
[Back pain in children]. Wiad Lek (2008) 0.75
Surveyor nuclease detection of mutations and polymorphisms of mtDNA in children. Pediatr Neurol (2010) 0.75
Uterus-like mass. Pol J Pathol (2010) 0.75
Apolipoprotein E genotype and LRP1 polymorphisms in patients with different clinical types of metachromatic leukodystrophy. Gene (2013) 0.75
[Multiple cerebral glioma or tumor dissemination via CSF pathways? Case report]. Neurol Neurochir Pol (2004) 0.75
New light on prions: putative role of co-operation of PrPc and Aβ proteins in cognition. Folia Neuropathol (2014) 0.75
[Direct surgical outcome of meningiomas obliterating the superior sagittal sinus]. Przegl Lek (2006) 0.75
[Sudden infant death syndrome--current opinions on etiology and pathogenesis]. Wiad Lek (2009) 0.75
[Juvenile dermatomyositis in 12 years old girl]. Wiad Lek (2005) 0.75
An attempt at evaluating borderline conditions of Parkinson's disease and its preclinical stage on the basis of clinical and morphological correlation. Folia Neuropathol (2002) 0.75
[Vertebral canal abscess as a complication of congenital sacral sinus in a two year old girl]. Neurol Neurochir Pol (2002) 0.75
Clinical and neuropathological picture of ethylmalonic aciduria - diagnostic dilemma. Folia Neuropathol (2011) 0.75
Synchrotron radiation based X-ray fluorescence shows changes in the elemental composition of the human substantia nigra in aged brains. Metallomics (2015) 0.75
[Neurocutaneous melanosis--case report]. Wiad Lek (2004) 0.75
Angelman syndrome and hypothyroidism - coincidence or unique correlation? Neuro Endocrinol Lett (2007) 0.75
Stereotactic biopsy in surgically inaccessible tumors with the use of "P.N." type frame. Ann Acad Med Stetin (2007) 0.75
Degeneration and calcification of the cervical endplate is connected with decreased expression of ANK, ENPP-1, OPN and TGF-β1 in the intervertebral disc. Pol J Pathol (2014) 0.75
Four-and-one-half years' experience in monitoring of reproducibility of an MR spectroscopy system--application of in vitro results to interpretation of in vivo data. J Appl Clin Med Phys (2014) 0.75
[Neuroimaging and clinical manifestations of herpes simplex encephalitis in children]. Neurol Neurochir Pol (2003) 0.75
[Herpes encephalitis at children]. Wiad Lek (2004) 0.75
CDG type Ia and congenital cytomegalovirus infection: two coexisting conditions. J Child Neurol (2009) 0.75
Giant schwannoma of the cheek--a comprehensive histological and immunohistochemical description of a rare tumour. Pol J Pathol (2009) 0.75
Topoisomerase IIα as a prognostic factor in pituitary tumors. Pol Arch Med Wewn (2014) 0.75
Xp21.2 contiguous gene syndrome due to deletion involving glycerol kinase and Duchenne muscular dystrophy loci. Neurol India (2010) 0.75
[Neurological picture and 1H MRS in 4 children with hypoparathyroidism]. Przegl Lek (2005) 0.75
[Morphological changes of the colon in patients with irritable bowel syndrome]. Przegl Lek (2012) 0.75
First step toward the "fingerprinting" of brain tumors based on synchrotron radiation X-ray fluorescence and multiple discriminant analysis. J Biol Inorg Chem (2011) 0.75
Leukoencephalopathy with macrocephaly and mild clinical course. Neurol Neurochir Pol (2004) 0.75
Expression of Bcl-2 and Bax protein in normal pineal gland in children and young adult. J Mol Histol (2006) 0.75
[Partial lipodystrophy with C3 complement deficiency in 8 years old girl]. Wiad Lek (2004) 0.75
Maternal phenylketonuria. Wiad Lek (2009) 0.75
[Nonfunctional pituitary adenoma and pulmonary sarcoidosis--a case report]. Przegl Lek (2002) 0.75
Is neuroradiological imaging sufficient for exclusion of intracranial hypertension in children? Intracranial hypertension syndrome without evident radiological symptoms. Acta Neurochir Suppl (2010) 0.75
PTTG and Ki-67 expression in pituitary adenomas. Przegl Lek (2016) 0.75
Malformations of cortical development in children: clinical manifestation, neuroimaging and neuropathology in selected cases. Folia Neuropathol (2006) 0.75
Biomechanical aspects of preoperative planning of skull correction in children with craniosynostosis. Acta Bioeng Biomech (2012) 0.75
[Pituitary tumors: hormonal status and immunohistochemical evaluation]. Przegl Lek (2003) 0.75
Clinical and radiologic features of unilateral and bilateral schizencephaly in polish pediatric patients. J Child Neurol (2013) 0.75
Hyperammonemia in children: on the crossroad of different disorders. Neurologist (2012) 0.75