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Category archives: Clinical guide

Bibliography essential for the consultation of pediatric neurology.

Posted byAlberto AlcantudJune 1, 2023June 1, 2023Posted inClinical method

What you need to the pediatric neurologist a school report?

Posted byAlberto AlcantudMay 21, 2023June 22, 2026Posted inEducational proc.

Metabolic diseases with dysmorphia.

In Vademecum Metabolicum there are different guides depending on the clinical scenario, including metabolic diseases that present with dysmorphia:

Posted byAlberto AlcantudMay 10, 2023June 22, 2026Posted inMetabolism

Diseases peroxisomal.

Posted byAlberto AlcantudMay 10, 2023June 22, 2026Posted inrare diseases, Metabolism, Neonatal, Neurodegenerative

Epilepsy and sleep.

Posted byAlberto AlcantudMay 2, 2023June 22, 2026Posted inEpilepsy, Dream

Newborn screening for SMA.

https://www.iislafe.es/es/sociedad/noticias/3163/la-fe-pondra-en-marcha-un-programa-piloto-de-cribado-neonatal-para-detectar-la-atrofia-muscular-espinal

Posted byAlberto AlcantudMay 2, 2023June 22, 2026Posted inNeurological diseases, rare diseases, Neurogenetics, Neuromuscular

Technologies aumentativas and alternative communication.

To implement an augmentative and alternative communication system, it is necessary to follow an implementation itinerary:

Posted byAlberto AlcantudApril 28, 2023June 22, 2026Posted inNeurorehabilitation, Health proc., Treatment

Videos of pediatric epileptic syndromes.

https://www.sciencedirect.com/science/article/abs/pii/S1525505013004083 Epilepsy diagnosis. Epilepsy. ILAE task force epilepsy classification. Genetics in epilepsy.

Posted byAlberto AlcantudApril 23, 2023May 2, 2023Posted inEpilepsy

Report neuropediátrico.

There are usually several types of clinical documents that can be issued by a hospital center:

Posted byAlberto AlcantudApril 19, 2023June 22, 2026Posted inHealth proc.

Down syndrome in mosaic.

Children with mosaic Down syndrome are difficult to diagnose. There is an international initiative and a pilot research study that can be used in case of clinical suspicion.

Posted byAlberto AlcantudApril 18, 2023April 18, 2023Posted inrare diseases, Neurogenetics

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