Suchergebnisse - "Green, Andrew"

PubPharm (9)

1

A scoring system predicting the clinical course of CLPB defect based on the foetal and neonatal presentation of 31 patients

enthalten in: Journal of inherited metabolic disease | 2017

von Pronicka, E. | Ropacka-Lesiak, M. | Trubicka, J. | +25

2

ALG6-CDG : a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

enthalten in: Journal of inherited metabolic disease | 2016

von Morava, E. | Tiemes, V. | Thiel, C. | +28

ErratumIn: J Inherit Metab Dis. 2016 Sep;39(5):759. - PMID 27498540

3

Erratum to : ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

enthalten in: Journal of inherited metabolic disease | 2016

von Morava, E. | Tiemes, V. | Thiel, C. | +28

ErratumFor: J Inherit Metab Dis. 2016 Sep;39(5):713-23. - PMID 27287710

4

Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

enthalten in: Journal of inherited metabolic disease | 2016

von Morava, E. | Tiemes, V. | Thiel, C. | +28

5

Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

enthalten in: Journal of inherited metabolic disease | 2016

von Morava, E. | Tiemes, V. | Thiel, C. | +28

6

ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

enthalten in: Journal of inherited metabolic disease | 2016

von Morava, E. | Tiemes, V. | Thiel, C. | +28

7

ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

enthalten in: Journal of inherited metabolic disease | 2016

von Morava, E. | Tiemes, V. | Thiel, C. | +28

8

Erratum to : ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

enthalten in: Journal of inherited metabolic disease | 8 August 2016

von Morava-Kozicz, E. | Tiemes, V. | Thiel, C. | +28

9

ALG6-CDG : a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

enthalten in: Journal of inherited metabolic disease | 10 June 2016

von Morava-Kozicz, E. | Tiemes, V. | Thiel, C. | +28

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