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Items: 5

1.

Protein-redistribution diet in a case of tyrosine hydroxylase enzyme deficiency.

Cassani E, Barichella M, Ferri V, Pusani C, Goldwurm S, Siri C, Zini M, Zorzi GS, Cereda E, Iorio L, Pinelli G, Sacilotto G, Pezzoli G.

Mov Disord. 2017 May;32(5):794-795. doi: 10.1002/mds.26963. Epub 2017 Mar 28. No abstract available.

PMID:
28370247
2.

An Indian Family with Tyrosine Hydroxylase Deficiency.

Goswami JN, Sankhyan N, Singhi PD.

Indian Pediatr. 2017 Jun 15;54(6):499-501.

3.

Good obstetric outcome in a patient with Segawa disease.

Watanabe T, Matsubara S.

Arq Neuropsiquiatr. 2012 Jul;70(7):559-60. No abstract available.

4.

Rationale for dopa-responsive CTNNB1/ß-catenin deficient dystonia.

Pipo-Deveza J, Fehlings D, Chitayat D, Yoon G, Sroka H, Tein I.

Mov Disord. 2018 Apr;33(4):656-657. doi: 10.1002/mds.27320. Epub 2018 Feb 13. No abstract available.

PMID:
29436745
5.

'Pyruvate dehydrogenase deficiency presenting as dystonia and responding to levodopa'.

Neubauer D, Frelih J, Zupancic N, Kopac S, Cindro-Heberle L.

Dev Med Child Neurol. 2005 Jul;47(7):504. No abstract available.

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