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Items: 2

1.

13-year diagnostic delay as cerebral palsy of an Iraqi patient with NBIA type 4.

Hadi AS, Saadi NW, Fahad QA.

Neurol Clin Pract. 2019 Jun;9(3):e22-e24. doi: 10.1212/CPJ.0000000000000622. No abstract available.

PMID:
31341721
2.

HTRA2 Defect: A Recognizable Inborn Error of Metabolism with 3-Methylglutaconic Aciduria as Discriminating Feature Characterized by Neonatal Movement Disorder and Epilepsy-Report of 11 Patients.

Kovacs-Nagy R, Morin G, Nouri MA, Brandau O, Saadi NW, Nouri MA, van den Broek F, Prokisch H, Mayr JA, Wortmann SB.

Neuropediatrics. 2018 Dec;49(6):373-378. doi: 10.1055/s-0038-1667345. Epub 2018 Aug 16.

PMID:
30114719

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