Suchergebnisse - "Ostergaard, E"

PubPharm (147)

1

One-minute sit-to-stand test as a quick functional test for people with COPD in general practice

enthalten in: NPJ primary care respiratory medicine | 2023

von Spence, J. | Brincks, J. | Løkke, A. | +2

2

A healthy individual with a homozygous PTCH2 frameshift variant : Are variants of PTCH2 associated with nevoid basal cell carcinoma syndrome?

enthalten in: Human genome variation | 2019

von Altaraihi, M. | Wadt, K. | Ek, J. | +2

3

Two transgenic mouse models for -subunit components of succinate-CoA ligase yielding pleiotropic metabolic alterations

enthalten in: The biochemical journal | 2016

von Kacso, G. | Ravasz, D. | Doczi, J. | +19

4

Physical training move mountains in COPD

enthalten in: Physiotherapy | 2016

von Østergaard, E. | Kristiansen, A. | Thomsen, P. | +1

5

Identification of novel locus at chromosome 3p12.3-q13.31 for autosomal recessive intellectual disability in a consanguineous family

enthalten in: Clinical genetics | 2014

von Dad, S. | Østergaard, E. | Wadt, K. | +3

6

Identification of novel locus at chromosome 3p12.3‐q13.31 for autosomal recessive intellectual disability in a consanguineous family

enthalten in: Clinical genetics | 2014

von Dad, S. | Østergaard, E. | Wadt, K. | +3

7

Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects : what we learned from 130 cases

enthalten in: Journal of inherited metabolic disease | 2012

von Koene, S. | Rodenburg, R. | van der Knaap, M. | +13

8

Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases

enthalten in: Journal of inherited metabolic disease | 2012

von Koene, S. | Rodenburg, R. | van der Knaap, M. | +13

9

Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases

enthalten in: Journal of inherited metabolic disease | 2012

von Koene, S. | Rodenburg, R. | van der Knaap, M. | +13

10

Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases

enthalten in: Journal of inherited metabolic disease | 2012

von Koene, S. | Rodenburg, R. | van der Knaap, M. | +13

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