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List of works by Lorena Monge-Galindo

A novel neurocutaneous syndrome: Legius syndrome. A case report

scientific article published in September 2014

A study of epilepsy according to the age at onset and monitored for 3 years in a regional reference paediatric neurology unit

scientific article published on 9 June 2016

Acute cerebellitis in paediatric patients: Our experience.

scientific article

Anti-NMDA receptor encephalitis in a four-year-old male

scientific article published on 01 July 2011

Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study

scientific article published on 10 February 2020

CHARGE syndrome and CHD7 gene mutation ⬇️

scientific article published on December 31, 2010

Changes in the demand for paediatric neurology care in a spanish tertiary care hospital over a 20-year period

scientific article published on 30 January 2013

Claude syndrome secondary to head trauma

scientific article published on 08 June 2018

Continuous monitoring of a guideline: Bell's palsy ⬇️

scientific article published on 01 March 2011

Descriptive study of symptomatic epilepsy by age of onset in patients with a 3-year follow-up at the Neuropaediatric Department of a reference centre.

scientific article published on 15 April 2016

Eclampsia as cause of seizure in a 12 year-old girl ⬇️

scientific article published on 03 April 2011

GNAO1 encephalopathy: further delineation of a severe neurodevelopmental syndrome affecting females.

scientific article

Idiopathic intracranial hypertension: Experience over 25 years and a management protocol

scientific article published on 13 October 2016

Intervertebral disc calcification as a cause of painful torticollis in children

scientific article published on 15 August 2018

Optic neuritis in paediatric patients: Experience over 27 years and a management protocol.

scientific article

Our experience with the aetiological diagnosis of global developmental delay and intellectual disability: 2006-2010.

scientific article published on 11 December 2013

Paroxysmal autonomic dysfunction of neonatal onset and medulloblastoma ⬇️

scientific article published on June 22, 2011

Prenatal encephalopathies of unknown origin. Our 19-years experience. To what extent must genetic and biochemical studies be carried out? ⬇️

scientific article published on March 4, 2011

Prognosis of non-symptomatic epilepsy in relation to their age of onset, monitored at a neuropediatric section of regional reference over a period of three years

scientific article

Prognosis of symptomatic epilepsies in relation to their age of onset, monitored at a neuropediatric section of regional reference over a period of three years

scientific article published in March 2016

Triplet expansion cytosine-guanine-guanine: Three cases of OMIM syndrome in the same family

scientific article published on 6 January 2016

[A descriptive study of non-symptomatic epilepsy according to age at onset at a Neuropediatric Section of regional reference]

scientific article published in November 2016

[Familial MECP2 duplication syndrome]

scientific article published on 01 April 2020

[Neurofibromatosis 1 and multiple familial cavernomatosis in an infant with episodic profuse sialorrhoea]

scientific article published on 01 October 2019

[Neurofibromatosis type 1 and attention-deficit disorder. Our current experience]

scientific article published on 01 January 2019

[Tuberculous hypophysitis mimicking Tolosa-Hunt syndrome].

scientific article

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