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46.
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Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy. [electronic resource] by
- Auranen, M
- Paetau, A
- Piirilä, P
- Pohju, A
- Salmi, T
- Lamminen, A
- Löfberg, M
- Mosegaard, S
- Olsen, R K
- Tyni, T
Producer: 20180316
In:
Neuromuscular disorders : NMD vol. 27
Availability: No items available.
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47.
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Prediction of disease severity in multiple acyl-CoA dehydrogenase deficiency: A retrospective and laboratory cohort study. [electronic resource] by
- van Rijt, Willemijn J
- Ferdinandusse, Sacha
- Giannopoulos, Panagiotis
- Ruiter, Jos P N
- de Boer, Lonneke
- Bosch, Annet M
- Huidekoper, Hidde H
- Rubio-Gozalbo, M Estela
- Visser, Gepke
- Williams, Monique
- Wanders, Ronald J A
- Derks, Terry G J
Producer: 20200916
In:
Journal of inherited metabolic disease vol. 42
Availability: No items available.
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53.
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54.
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Myopathy with MTCYB mutation mimicking Multiple Acyl-CoA Dehydrogenase Deficiency. [electronic resource] by
- Kaphan, E
- Bou Ali, H
- Gastaldi, M
- Acquaviva, C
- Vianey-Saban, C
- Rouzier, C
- Fragaki, K
- Bannwarth, S
- Paquis-Flucklinger, V
- Romero, N
- Behin, A
- Lombès, A
- Jardel, C
- Rigal, O
- Laforêt, P
Producer: 20190213
In:
Revue neurologique vol. 174
Availability: No items available.
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