I. Pascual‐Castroviejo

发表

I. Pascual‐Castroviejo, 2000 .

Do cutaneous hemangiomas and internal vascular anomalies follow the same evolution?

S. Pascual-Pascual, J. Viano, S. Pascual-Pascual, 2003, Neurology.

Flaccid paraplegia as complication of umbilical artery catheterization.

A. Martínez-Bermejo, R. Escribá, I. Pascual‐Castroviejo, 1993, Pediatric neurology.

Hemangiomas of the head, neck, and chest with associated vascular and brain anomalies: a complex neurocutaneous syndrome.

I. Pascual-Castroviejo, J. García-Peñas, S. Pascual-Pascual, 1996, AJNR. American journal of neuroradiology.

Cutaneous thoracic hemangioma and internal vascular anomalies

I. Pascual‐Castroviejo, L. García-Guereta, S. I. Pascual-Pascual, 2005, Journal of Pediatric Neurology.

Vascular Birthmarks of Infancy: Phace Association (Pascual-Castroviejo Type II Syndrome) and Cobb Syndrome

I. Pascual-Castroviejo, I. Pascual‐Castroviejo, 2008 .

Facial Hemangioma and Hemispheric Migration Disorder: Presentation of 5 Patients

S. Pascual-Pascual, J. López-Gutiérrez, J. Viano, 2007, American Journal of Neuroradiology.

Klippel-Tranaunay, Parkes Weber and Sturge-Weber Syndromes (Including Kasabach-Merrit Phenomena)

M. Ruggieri, O. Konez, I. Pascual‐Castroviejo, 2008 .

Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes

M. Ruggieri, C. Rocco, I. Pascual‐Castroviejo, 2008 .

Hypohidrotic Ectodermal Dysplasia (HED)

I. Pascual-Castroviejo, M. Ruggieri, I. Pascual‐Castroviejo, 2008 .

Neurofibromatosis type 1 with external genitalia involvement presentation of 4 patients.

M. Cisternino, S. Savasta, J. López-Gutiérrez, 2008, Journal of pediatric surgery.

Chondrodysplasia Punctata (Cdp) Conradi-Hunermann-Happle Type (Cdpx2)

M. Ruggieri, I. Pascual‐Castroviejo, 2008 .

Hypomelanosis of Ito. Neurological Complications in 34 Cases

C. Herrero, I. Pascual‐Castroviejo, Luisa López-Rodriguez, 1988, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[Cutis marmorata telangiectatica congenita. Associated abnormalities].

M. C. Roche Herrero, J. López-Herce Cid, I. Pascual‐Castroviejo, 1985, Anales espanoles de pediatria.

Becker's Nevus Syndrome

A. Polizzi, F. Lacarrubba, A. Verzì, 2018, Journal of Pediatric Neurology.

Encephalocraniocutaneous Lipomatosis (Haberland Syndrome)

S. Jóźwiak, I. Pascual‐Castroviejo, 2008 .

Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome)

A. Polizzi, F. Lacarrubba, G. Micali, 2018, Journal of Pediatric Neurology.

Focal Dermal Hypoplasia Syndrome (Goltz Syndrome)

I. Pascual-Castroviejo, M. Ruggieri, I. Pascual‐Castroviejo, 2008 .

Sturge-Weber syndrome: study of 40 patients.

I. González-Casado, C. Díaz-González, I. Pascual‐Castroviejo, 1993, Pediatric neurology.

Sturge-Weber Syndrome. Study of 55 Patients

I. Pascual-Castroviejo, S. Pascual-Pascual, J. Viano, 2008, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Congenital vascular malformations in childhood.

I. Pascual-Castroviejo, I. Pascual‐Castroviejo, 2008, Handbook of clinical neurology.

Congenital vascular malformations in childhood.

I. Pascual-Castroviejo, S. Pascual-Pascual, I. Pascual‐Castroviejo, 2002, Seminars in pediatric neurology.

Hypomelanosis of Ito and Related Disorders (Pigmentary Mosaicism)

M. Ruggieri, I. Pascual‐Castroviejo, 2008 .

Hypomelanosis of ITO. A study of 76 infantile cases

S. Pascual-Pascual, A. Martínez-Bermejo, J. Arcas, 1998, Brain and Development.

Arteriovenous malformation in hypomelanosis of Ito

I. Pascual‐Castroviejo, C. Roche, A. Vega, 1996, Brain and Development.

Incontinentia pigmenti: MR demonstration of brain changes.

J. García-Peñas, V. Martínez Fernández, M. Roche, 1994, AJNR. American journal of neuroradiology.

Sturge-Weber syndrome without facial nevus.

S. Pascual-Pascual, J. Coya, J. Viano, 1995, Neuropediatrics.

Hypomelanosis of Ito

A. Polizzi, S. Savasta, F. Lacarrubba, 1981, Journal of Pediatric Neurology.

Progeria and Progeroid Syndromes (Premature Ageing Disorders)

I. Pascual-Castroviejo, M. Ruggieri, I. Pascual‐Castroviejo, 2008 .

Anterior sacral meningocele: review of the literature.

I. Pascual-Castroviejo, C. Scavone, A. Pérez-Higueras, 1983, Surgical neurology.

The Association of Extracranial and Intracranial Vascular Malformations in Children

I. Pascual-Castroviejo, I. Pascual‐Castroviejo, 1985, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Neurofibromatosis type 1 & Related Disorders

M. Upadhyaya, M. Ruggieri, C. Rocco, 2008 .

Primary intracranial arachnoidal cysts

M. García Blázquez, M. Roche, J. Arcas, 1991, Child's Nervous System.

Lesch-Nyhan Syndrome

M. Ruggieri, I. Pascual‐Castroviejo, 2008 .

Cerebro‐Facio‐Thoracic Dysplasia: Report of Three Cases

F. Mulas, I. Pascual‐Castroviejo, A. Tendero, 1975, Developmental medicine and child neurology.

Pascual-Castroviejo type II syndrome (P-CIIS). Importance of the presence of persistent embryonic arteries

I. Pascual-Castroviejo, S. Pascual-Pascual, J. Alvarez-Linera, 2011, Child's Nervous System.

Identification of de novo deletions at the NF1 gene: no preferential paternal origin and phenotypic analysis of patients

M. C. Valero, I. Pascual-Castroviejo, E. Velasco, 1997, Human Genetics.

[Cerebrofaciothoracic dysplasia (Pascual-Castroviejo type I syndrome): presentation of two new patients].

R. Velázquez-Fragua, S. P. Pascual Pascual, I. Pascual‐Castroviejo, 2007, Neurologia.

Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy.

M. T. Medina, R. Olsen, G. Pineda, 2008, American journal of human genetics.

Speckled Lentiginous Nevus Syndrome

A. Polizzi, F. Lacarrubba, G. Micali, 2018, Journal of Pediatric Neurology.

Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome)

A. Polizzi, F. Lacarrubba, G. Micali, 2018, Journal of Pediatric Neurology.

Significance of tuber size for complications of tuberous sclerosis complex.

I. Pascual-Castroviejo, S. Pascual-Pascual, J. Hernández-Moneo, 2013, Neurologia.

Neurosurgical treatment of tuberous sclerosis complex lesions

I. Pascual-Castroviejo, I. Pascual‐Castroviejo, 2011, Child's Nervous System.

Costello Syndrome and the Ras-Extracellular Signal Regulated Kinase (ERK) Pathway

M. Ruggieri, I. Pascual‐Castroviejo, 2008 .

[Munchausen syndrome by proxy: report of one case with epilepsy].

A. Martínez-Bermejo, A. Fernández-Jaén, I. Pascual‐Castroviejo, 1998, Revista de neurologia.

AHI1 gene mutations cause specific forms of Joubert syndrome–related disorders

E. Bertini, F. Brancati, E. Valente, 2006, Annals of neurology.

Primary Degeneration of the Granular Layer of the Cerebellum. A Study of 14 Patients and Review of the Literature

I. Pascual-Castroviejo, S. Pascual-Pascual, A. Martínez-Bermejo, 1994, Neuropediatrics.

Dandy-Walker malformation: analysis of 38 cases

I. Pascual-Castroviejo, M. Roche, S. Pascual-Pascual, 1991, Child's Nervous System.

Total craniopagus twins.

C. Morales, F. Villarejo, I. Pascual‐Castroviejo, 1981, Child's brain.

Vacuolating megalencephalic leukoencephalopathy: 24 year follow-up of two siblings.

I. Pascual-Castroviejo, S. Pascual-Pascual, M. S. van der Knaap, 2005, Neurologia.

Electroretinogram in Duchenne/Becker muscular dystrophy.

I. Pascual-Castroviejo, J. Molano, S. P. Pascual Pascual, 1998, Pediatric neurology.

Cutaneous, mediastinal and hepatic hemangiomas in a girl followed during 12 years.

P. Jara, R. Velázquez-Fragua, M. Parrón Pajares, 2011, Neuropediatrics.

[Cutaneous haemangioma associated with a hepatic haemangioma and neurofibromatosis type 1 (NF1)].

P. Cortés, J. Fernández-Cuadrado, S. P. Pascual Pascual, 2002, Revista de neurologia.

[Syringomyelia, Chiari's malformation and scoliosis in a patient with type 1 neurofibromatosis].

A. Fernández-Jaén, I. Pascual‐Castroviejo, B. Calleja‐Pérez, 1998, Anales espanoles de pediatria.

[Neurofibromatosis type 2 (NF2). Study of 7 patients].

J. Viano, S. Pascual-Pascual, I. Pascual‐Castroviejo, 2009, Neurologia.

Oculocerebrocutaneous (Delleman) syndrome: report of two cases.

P. Lapunzina, I. Pascual-Castroviejo, S. Pascual-Pascual, 2005, Neuropediatrics.

Bilateral arachnoid cysts, seizures and severe encephalopathy: case report.

S. Pascual-Pascual, I. Pascual‐Castroviejo, 1994, Neuropediatrics.

Radiological and anatomical aspects of the cranial metastases of neuroblastomas

I. Pascual‐Castroviejo, V. Lopez-Martin, T. Rodríguez-Costa, 1975, Neuroradiology.

Linear scleroderma (morphoea) “en coup de sabre”

I. Pascual-Castroviejo, M. Ruggieri, I. Pascual‐Castroviejo, 2008 .

[A case of Dyggve-Melchior-Clausen's syndrome (author's transl)].

C. Casas, I. Pascual‐Castroviejo, T. Rodríguez Costa, 1976, Anales espanoles de pediatria.

Optic glioma with progressive occlusion of the aqueduct of sylvius in monozygotic twins with neurofibromatosis

A. Verdú, F. Villarejo, I. Pascual‐Castroviejo, 1988, Brain and Development.

Fronto-nasal dysplasia and lipoma of the corpus callosum

A. Pérez-Higueras, S. Pascual-Pascual, I. Pascual‐Castroviejo, 1985, European Journal of Pediatrics.

Childhood choroid plexus neoplasms

A. Pérez-Higueras, C. Morales, S. Pascual-Pascual, 1983, European Journal of Pediatrics.

Facial haemangioma, agenesis of the internal carotid artery and dysplasia of cerebral cortex: case report

J. Viano, S. Pascual-Pascual, V. Martínez, 1995, Neuroradiology.

Focal cortical dysplasia. Clinical-radiological-pathological associations.

S. Pascual-Pascual, J. Hernández-Moneo, J. Viano, 2012, Neurologia.

Posterior fossa tumors in children with neurofibromatosis type 1 (NF1)

S. Pascual-Pascual, F. Carceller, J. Viano, 2010, Child's Nervous System.

Posterior fossa tumors in children with neurofibromatosis type 1 (NF1)

I. Pascual‐Castroviejo, 2010, Child's Nervous System.

Neurofibromatosis type 1 (NF1) associated with tumor of the corpus callosum

S. Pascual-Pascual, I. Pascual‐Castroviejo, 2012, Child's Nervous System.

Complications of Neurofibromatosis Type 1 in a Series of 197 Children

I. Pascual‐Castroviejo, 1992 .

24-year preoperative evolution of a temporal astrocytoma

F. Carceller, M. G. Blázquez, I. Pascual‐Castroviejo, 1996, Child's Nervous System.

[Muscle-eye-brain disease. Presentation of one case with genetic study].

M. Bayés, B. Cormand, I. Pascual-Castroviejo, 2005, Neurologia.

Vascular and nonvascular intracranial malformations associated with external capillary hemangiomas

I. Pascual-Castroviejo, I. Pascual‐Castroviejo, 2004, Neuroradiology.

Seizures of Idiopathic Generalized Epilepsies

M. T. Medina, María Elisa Alonso, A. Delgado-Escueta, 2005, Epilepsia.

[Effects of corticosteroids in the management of Duchenne muscular dystrophy: our experience].

S. Rafia, S. Pascual-Pascual, I. Pascual‐Castroviejo, 2002, Anales espanoles de pediatria.

Hydatid cyst of the posterior fossa: case report.

F. Esteban, J. Arcas, M. G. Blázquez, 1983, Neurosurgery.

[Comorbid disorders of the attention deficit with hyperactivity disorder].

I. Pascual-Castroviejo, I. Pascual‐Castroviejo, 2002, Revista de neurologia.

[Incontinentia pigmenti: clinical and neuroimaging findings in a series of 12 patients].

S. Pascual-Pascual, R. Velázquez-Fragua, V. Martínez, 2006, Neurologia.

NOP08 Aqueductal stenosis in the neurofibromatosis type 1 (NF1): presentation of 19 infantile patients

S. Pascual-Pascual, F. Carceller, J. Viano, 2007 .

[Aqueductal stenosis in the neurofibromatosis type 1. Presentation of 19 infantile patients].

F. Carceller-Benito, J. Viano, R. Velázquez-Fragua, 2007, Revista de neurologia.

Bilateral Obstruction of the Vertebral Arteries in a Three‐year‐old Child

F. Mulas, M. Roche, I. Pascual‐Castroviejo, 1977, Developmental medicine and child neurology.

Maple Syrup Urine Disease Variant Form: Presentation with Psychomotor Retardation and CT Scan Abnormalities

M. Ugarte, A. Martínez-Bermejo, J. López-Herce, 1985, Acta paediatrica Scandinavica.

Nevus of OTA

M. Ruggieri, I. Pascual‐Castroviejo, Martino Ruggieri, 2008 .

[Extracranial and intracranial vascular abnormalities and nevus of Ota in the same family].

S. Pascual-Pascual, J. Viano, F. Moreno, 2003, Neurologia.

Is Cerebral Arteritis the Cause of the Landau-Kleffner Syndrome? Four Cases in Childhood with Angiographic Study

I. Pascual‐Castroviejo, A. Bermejo, A. P. Higueras, 1992, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[Status epilepticus in childhood].

A. Martínez-Bermejo, S. Pascual-Pascual, I. Pascual‐Castroviejo, 1997, Neurología.

Cutaneous Hemangioma Associated With Persistence of the Trigeminal and Both Proatlantal Arteries

I. Pascual-Castroviejo, J. López-Gutiérrez, I. Pascual‐Castroviejo, 2007, Journal of child neurology.

Persistence of the Hypoglossal Artery and Partial Agenesis of the Cerebellum

J. López-Terradas, A. Martínez-Bermejo, C. Casas, 1975 .

Neurocutaneous Disorders: Cutaneous hemangiomas: vascular anomaly complex

I. Pascual‐Castroviejo, 2004 .

Cobb Syndrome: Case Report

S. Pascual-Pascual, R. Frutos, J. Viano, 2002, Journal of child neurology.

Major and Minor Arterial Malformations in Patients With Cutaneous Vascular Abnormalities

S. Pascual-Pascual, J. López-Gutiérrez, J. Viano, 2010, Journal of child neurology.

Cutaneous hemangiomas and vascular abnormalities: persistence of embryonic vascularization.

S. Pascual-Pascual, I. Pascual‐Castroviejo, J. Delgado, 2007, AJNR. American journal of neuroradiology.

[Cutaneous hemangiomas and vascular malformations and associated pathology (Pascual-Castroviejo type II syndrome). Study of 41 patients].

S. Pascual-Pascual, J. López-Gutiérrez, R. Palencia, 2005, Revista de neurología (Ed. impresa).

Vascular changes in cerebellar developmental defects

I. Pascual‐Castroviejo, 2004, Neuroradiology.

Unilateral somatic and intracranial hypoplasia.

J. Viano, S. Pascual-Pascual, V. Martínez, 1997, Neuropediatrics.

Association of Cutaneous Red-to-Purple Hemangiomas with Leptomeningeal Hemangiomas. A Clinical Study of Two Patients

S. Pascual-Pascual, J. López-Gutiérrez, J. Tovar, 2010, Neuropediatrics.

SjÖgren-Larsson Syndrome

M. Ruggieri, I. Pascual‐Castroviejo, 2008 .

Safety of botulinum toxin type A in children younger than 2 years.

I. Pascual-Castroviejo, S. Pascual-Pascual, I. Pascual‐Castroviejo, 2009, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Status epilepticus‐induced brain damage and opercular syndrome in childhood

I. Pascual-Castroviejo, S. Pascual-Pascual, W. Peña, 1999 .

The Spectrum of HGPRT Deficiency

A. Buño, R. Torres, J. Puig, 1998 .

[Cervical spinal cord compression in chondrodysplasia punctata: report of two cases].

J. García-Peñas, J. Hernández-Moneo, S. Pascual-Pascual, 2004, Revista de neurologia.

[Benign neonatal convulsions. Review of 23 cases].

M. C. Roche Herrero, V. López Martín, I. Pascual‐Castroviejo, 1996, Neurologia.

[Occipital leptomeningeal angiomatosis without facial angioma. Could it be considered a variant of Sturge-Weber syndrome?].

A. Martínez-Bermejo, I. Polanco, J. Viano, 2000, Revista de neurologia.

Treating Spastic Equinus Foot from Cerebral Palsy with Botulinum Toxin Type A: What Factors Influence the Results?: An Analysis of 189 Consecutive Cases

S. Pascual-Pascual, P. G. Garcia Ruiz, I. Pascual‐Castroviejo, 2011, American journal of physical medicine & rehabilitation.

Status epilepticus-induced brain damage and opercular syndrome in childhood.

S. Pascual-Pascual, W. Peña, M. Talavera, 1999, Developmental medicine and child neurology.

Ataxia-telangiectasia (A-T). Contribution with eighteen personal cases

S. Pascual-Pascual, I. Pascual‐Castroviejo, V. Lopez-Martin, 1981, Brain and Development.

MLC1 is associated with the Dystrophin-Glycoprotein Complex at astrocytic endfeet

F. Muntoni, W. Kamphorst, G. Scheper, 2007, Acta Neuropathologica.

[Opercular syndrome after bilateral cerebral surgery: presentation of a case report].

S. Pascual-Pascual, I. Pascual‐Castroviejo, 2004, Revista de neurologia.

Nicardipine in the Treatment of Acquired Aphasia and Epilepsy

I. Pascual‐Castroviejo, 1990, Developmental medicine and child neurology.

Clinical Pictures of Vascular Pathology in Children

I. Pascual‐Castroviejo, 1992 .

Progressive facial hemiatrophy (parry-romberg syndrome)

D. Restivo, P. Milone, I. Pascual‐Castroviejo, 2008 .

[Hypothalamic hamartomas: control of seizures after partial removal in one case].

J. García-Segura, J. Viano, S. P. Pascual Pascual, 2000, Revista de neurologia.

An overview of L‐2‐hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype–phenotype study

D. Zafeiriou, J. Celli, J. D. den Dunnen, 2010, Human mutation.

Unilateral polymicrogyria: a common cause of hemiplegia of prenatal origin

S. Pascual-Pascual, J. Viano, R. Palencia, 2001, Brain and Development.

Congenital cytomegalovirus infection and cortical/subcortical malformations

S. Pascual-Pascual, J. López, I. Pascual‐Castroviejo, 2012 .

Congenital cytomegalovirus infection and cortical/subcortical malformations

S. Pascual-Pascual, R. Velázquez-Fragua, I. Pascual‐Castroviejo, 2012 .

Burkitt's lymphoma presenting as Tolosa-Hunt syndrome.

Á. Carrasco Sanz, V. Martínez Fernández, C. Sánchez Pina, 1993, Pediatric Neurology.

[Nicardipine-induced gingival hyperplasia].

S. P. Pascual Pascual, I. Pascual‐Castroviejo, 1997, Neurologia.

[Schilder's diffuse myelinoclastic sclerosis].

A. Martínez-Bermejo, A. Fernández-Jaén, J. Arcas, 2001, Revista de neurologia.

[Behr's syndrome. a report of seven cases].

I. Pascual‐Castroviejo, M. Pizzatto, 2001, Revista de neurologia.

Diplegia due to Transcranial Knife-Blade Injury in a 20-Month-Old Child

I. Pascual-Castroviejo, S. Pascual-Pascual, J. Viano, 2006, Journal of child neurology.

Neuronal Plasticity

I Pascual-Castroviejo, I. Pascual‐Castroviejo, Our Neuropharmacology Correspondent, 1973, Nature.

[Syringohydromyelia. Report of a case which resolved spontaneously].

S. Rafia, I. Pascual‐Castroviejo, 2001, Revista de neurología (Ed. impresa).

[Neurological changes in Giedion's syndrome (tricho-rhinophalagia type I)].

J. López-Herce Cid, I. Pascual‐Castroviejo, O. Ramírez Balza, 1985, Anales espanoles de pediatria.

Treatment of Acquired Aphasia and Epilepsy

T. Deonna, E. Roulet, I. Pascual‐Castroviejo, 1991, Developmental medicine and child neurology.

Schizencephaly: A study of 16 patients

S. Pascual-Pascual, J. Viano, D. Quiñones, 2012 .

Schizencephaly: a study of 16 patients.

S. Pascual-Pascual, J. Viano, D. Quiñones, 2012, Neurologia.

Focal cortical dysplasia. Clinical-radiological-pathological associations (cid:2)

J. Hernández-Moneo, J. Viano, D. Quiñones, 2023 .

T-STAR gene: fine mapping in the candidate region for childhood absence epilepsy on 8q24 and mutational analysis in patients

K. Yamakawa, P. Shah, A. Delgado-Escueta, 2001, Epilepsy Research.

Intramedullary dermoid of the cervical spinal cord in a child.

A. Verdú, F. Villarejo, M. De La Cruz, 1986, Journal of Neurology Neurosurgery & Psychiatry.

[Subependymal giant cell astrocytoma in tuberous sclerosis complex. A presentation of eight paediatric patients].

I. Pascual-Castroviejo, S. Pascual-Pascual, J. Hernández-Moneo, 2010, Neurologia.

[Cerebellar ataxia of Norman-Jaeken. Presentation of seven Spanish patients].

I. Pascual-Castroviejo, S. Quijano-roy, S. Pascual-Pascual, 2006, Revista de neurologia.

Functional Basis of Posterior Fossa Tumor Symptoms and Signs

I. Pascual‐Castroviejo, 1993 .

Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria

I. Scheffer, Siddharth Srivastava, B. Bourgeois, 2023, JAMA neurology.

RPGRIP1L mutations are mainly associated with the cerebello‐renal phenotype of Joubert syndrome‐related disorders

T. Sanger, E. Bertini, M. Koenig, 2008, Clinical genetics.

Schizencephaly: A study of 16 patients

S. Pascual-Pascual, J. Viano, D. Quiñones, 2012 .

Neurocutaneous Disorders: Cutaneous hemangiomas: vascular anomaly complex

I. Pascual‐Castroviejo, 2004 .

Cerebellar hypoplasia with heterotopic purkinje cells in the molecular layer and preservation of the granule layers associated with severe encephalopathy. A new entity?

S. Pascual-Pascual, C. Katsetos, H. Urich, 2003, Neuropediatrics.

[Kabuki make-up syndrome. A report of 18 Spanish cases].

S. Pascual-Pascual, R. Palencia, R. Velázquez-Fragua, 2005, Revista de neurología (Ed. impresa).

[Williams-Beuren syndrome: presentation of 82 cases].

F. Moreno Granado, R. Gracia‐Bouthelier, S. Pascual-Pascual, 2004, Anales de pediatria.

‘Congenital disorders of glycosylation syndromes’

I. Pascual‐Castroviejo, 2002, Developmental medicine and child neurology.

Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes

I. Pascual‐Castroviejo, Concezio Di Rocco, Martino Ruggieri, 2008 .

Choroid Plexus Papillomas of the Fourth Ventricle

M. Roche, F. Villarejo, I. Pascual‐Castroviejo, 1982 .

Significance of tuber size for complications of tuberous sclerosis complex.

S. Pascual-Pascual, J. Hernández-Moneo, J. Viano, 2013 .

Single fibre electromyography in central core disease

J. López-Terradas, I. Pascual‐Castroviejo, M. Ferrer, 1979, Journal of neurology, neurosurgery, and psychiatry.

Sturge-Weber syndrome: study of 55 patients.

S. Pascual-Pascual, J. Viano, R. Velázquez-Fragua, 2008, The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques.

Optic gliomas in neurofibromatosis type 1 (NF-1). Presentation of 31 cases.

V. López Martín, A. Martínez Bermejo, S. P. Pascual Pascual, 1994, Neurologia.

Focal cortical dysplasia. Clinical-radiological-pathological associations.

S. Pascual-Pascual, J. Hernández-Moneo, J. Viano, 2012 .