PUBLICACIÓN

Idiopathic intracranial hypertension. Review of our experience in the last eight years (2016-2023)

ACCEDER A LA PUBLICACIÓN: Scopus Dialnet

C. Torres Díaz, Cristina Cáceres Marzal, M.D. Sardina González, R. Real Terrón

2024 REVISTA DE NEUROLOGIA

Medicine (miscellaneous) (Q3), Neurology (clinical) (Q3)

JCR: 0.8

SJR: 0.304

CITAS

0

DOI

10.33588/rn.7903.2024112

EID

2-s2.0-85199015255

ISSN

0210-0010

AUTORES DE LA UEX

Cristina Cáceres Marzal

OTRAS PUBLICACIONES DE INTERÉS

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Clinical And Molecular Profiling In Gnao1 Permits Phenotype–genotype Correlation
Idiopathic Intracranial Hypertension. Review Of Our Experience In The Last Eight Years (2016-2023)
Clinical And Molecular Profiling In Gnao1 Permits Phenotype–genotype Correlation
Idiopathic Intracranial Hypertension. Review Of Our Experience In The Last Eight Years (2016-2023)
Clinprior: An Algorithm For Diagnosis And Novel Gene Discovery By Network-Based Prioritization
Idiopathic Intracranial Hypertension. Review Of Our Experience In The Last Eight Years (2016-2023)
Clinprior: An Algorithm For Diagnosis And Novel Gene Discovery By Network-Based Prioritization
Genetic Diagnosis Of Basal Ganglia Disease In Childhood
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Management And Monitoring Of Patients With Duchenne Disease
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Central Nervous System Chemotoxicity During Treatment Of Pediatric Acute Lymphoblastic Leukemia/lymphoma
Methotrexate-Induced Subacute Neurotoxicity In A Child With Acute Lymphoblastic Leukemia Carrying Genetic Polymorphisms Related To Folate Homeostasis
Central Nervous System Chemotoxicity During Treatment Of Pediatric Acute Lymphoblastic Leukemia/lymphoma
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Idiopathic Focal Epilepsies In Childhood. Diagnostic Difficulties
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Idiopathic Focal Epilepsies In Childhood. Diagnostic Difficulties
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Non-Verbal Learning Disorders: A Clinical Study And Pharmacological Treatment
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Decreased Corneal Opacity And Improved Vision In A Patient With Mucopolysaccharidosis I (Hurler-Scheie) Treated With Enzyme Replacement Therapy (Laronidase, Aldurazyme®)
Non-Verbal Learning Disorders: A Clinical Study And Pharmacological Treatment
Decreased Corneal Opacity And Improved Vision In A Patient With Mucopolysaccharidosis I (Hurler-Scheie) Treated With Enzyme Replacement Therapy (Laronidase, Aldurazyme®)
Early Response To Idursulfase Treatment In A 3 Year-Old Boy Affected Of Hunter Syndrome
Decreased Corneal Opacity And Improved Vision In A Patient With Mucopolysaccharidosis I (Hurler-Scheie) Treated With Enzyme Replacement Therapy (Laronidase, Aldurazyme®)
Early Response To Idursulfase Treatment In A 3 Year-Old Boy Affected Of Hunter Syndrome
Early Mitochondrial Dysfunction In An Infant With Alexander Disease
Early Response To Idursulfase Treatment In A 3 Year-Old Boy Affected Of Hunter Syndrome
Early Mitochondrial Dysfunction In An Infant With Alexander Disease
Holt-Oram Syndrome [4]
Early Mitochondrial Dysfunction In An Infant With Alexander Disease
Holt-Oram Syndrome [4]
Hair With A Double Crown And Dilatation Of Virchow-Robin Spaces: A Proposal For A New Neurocutaneous Association
Holt-Oram Syndrome [4]
Hair With A Double Crown And Dilatation Of Virchow-Robin Spaces: A Proposal For A New Neurocutaneous Association
Zellweger Syndrome. Reports On Two New Cases
Hair With A Double Crown And Dilatation Of Virchow-Robin Spaces: A Proposal For A New Neurocutaneous Association
Zellweger Syndrome. Reports On Two New Cases
Clinical And Molecular Profiling In Gnao1 Permits Phenotype–genotype Correlation
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