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Publications by Christian Matula

Initial Diagnosis of the Congenital Disorder of Glycosylation PMM2-CDG (CDG1a) in a 4-Year-Old Girl After Neurosurgical Intervention for Cerebral Hemorrhage

Journal of Neurosurgery: Pediatrics
Child HealthPerinatologyNeurologyMedicinePediatricsSurgery
2014English

Related publications

Pmm2-CDG

2020English

Anesthetic Management of a Boy With Congenital Disorder of Glycosylation (CDG) I-X

International Journal of Clinical Medicine
2011English

Further Delineation of the Phenotype of Congenital Disorder of Glycosylation DPAGT1-CDG (CDG-Ij) Identified by Homozygosity Mapping

JIMD Reports
Internal MedicineGeneticsMolecular BiologyBiochemistryEndocrinologyMetabolismDiabetes
2011English

Nutritional Therapies in Congenital Disorders of Glycosylation (CDG)

Nutrients
NutritionFood ScienceDietetics
2017English

Congenital Disorder of Glycosylation Type Ia (CDG-Ia): Phenotypic Spectrum of the R141h/F119l Genotype

Archives of Disease in Childhood
Child HealthPediatricsPerinatology
2001English

Congenital Disorder of Glycosylation

2020English

Child Neurology: A Case of PMM2-CDG (CDG 1a) Presenting With Unusual Eye Movements

Neurology
Neurology
2012English

P89 Toxic Epidermal Necrolysis in a 4 Year Old Girl in the UAE

2019English

Early Initial Diagnosis of Gardner Syndrome in a 12-Year-Old Boy

Advances in Computed Tomography
2013English

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