U. Werlauff: search on Z-Library

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1

Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutations

Witting, Nanna, Werlauff, Ulla, Duno, Morten, Vissing, John

Journal:

Year:

2016

Language:

english

File:

PDF, 481 KB

english, 2016

2

A randomized comparative study of two methods for controlling Tendo Achilles contracture in Duchenne muscular dystrophy

Sylvia A. Hyde, Ida Fløytrup, Sara Glent, Anna-Karin Kroksmark, Betty Salling, Birgit F. Steffensen, Ulla Werlauff, Mogens Erlandsen

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 184 KB

english, 2000

3

Collagen XII myopathy with rectus femoris atrophy and collagen XII retention in fibroblasts

Witting, Nanna, Krag, Thomas, Werlauff, Ulla, Duno, Morten, Oestergaard, Sofie Thuroe, Dahlqvist, Julia Rebecka, Vissing, John

Journal:

Year:

2018

Language:

english

File:

PDF, 1.10 MB

english, 2018

4

Bereaved Parents More Satisfied With the Care Given to Their Child With Severe Spinal Muscular Atrophy Than Nonbereaved

Hjorth, Elin, Kreicbergs, Ulrika, Sejersen, Thomas, Jeppesen, Jørgen, Werlauff, Ulla, Rahbek, Jes, Lövgren, Malin

Journal:

Journal of Child Neurology

Year:

2018

Language:

english

File:

PDF, 221 KB

english, 2018

5

T.P.1.05 Is a reduced muscle test sufficient to give an overall impression of muscle function in spinal muscle atrophy II?

Journal:

Neuromuscular Disorders

Year:

2008

Language:

english

File:

PDF, 49 KB

english, 2008

6

T.P.1.07 Egen classification revisited in SMA

B.F. Steffensen, A. Mayhew, A. Aloysius, M. Eagle, E. Mercuri, S. Messina, E. Mazzone, A. Nadeau, M. Main, E. Scott, U. Werlauff, B. Werge, A.M. Glanzmann, F. Muntoni

Journal:

Neuromuscular Disorders

Year:

2008

Language:

english

File:

PDF, 63 KB

english, 2008

7

Physical characteristics and applicability of standard assessment methods in a total population of spinal muscular atrophy type II patients

U. Werlauff, B.F. Steffensen, S. Bertelsen, I. Fløytrup, B. Kristensen, B. Werge

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 333 KB

english, 2010

8

P3.3 Does muscle strength deteriorate over time in Spinal muscular atrophy type II and III? Fifteen years follow up study in 22 patients with SMA II and 9 patients with SMA III

U. Werlauff, J. Vissing, B.F. Steffensen

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 59 KB

english, 2011

9

Longitudinal data analysis: an application to construction of a natural history profile of Duchenne muscular dystrophy

Sylvia A Hyde, Birgit F Steffensen, Ida Fløytrup, Sara Glent, Anna-Karin Kroksmark, Betty Salling, Ulla Werlauff, Mogens Erlandsen

Journal:

Neuromuscular Disorders

Year:

2001

Language:

english

File:

PDF, 171 KB

english, 2001

10

Change in muscle strength over time in spinal muscular atrophy types II and III. A long-term follow-up study

Werlauff, U., Vissing, J., Steffensen, B.F.

Journal:

Neuromuscular Disorders

Year:

2012

Language:

english

File:

PDF, 293 KB

english, 2012

11

Fatigue in patients with spinal muscular atrophy type II and congenital myopathies: evaluation of the fatigue severity scale

Werlauff, Ulla, HÃ¸jberg, A., Firla-Holme, R., Steffensen, B. F., Vissing, J.

Journal:

Quality of Life Research

Year:

2014

Language:

english

File:

PDF, 274 KB

english, 2014

12

Frequency and phenotype of patients carrying TPM2 and TPM3 gene mutations in a cohort of 94 patients with congenital myopathy

Citirak, Gülsenay, Witting, Nanna, Duno, Morten, Werlauff, Ulla, Petri, Helle, Vissing, John

Journal:

Neuromuscular Disorders

Year:

2014

Language:

english

File:

PDF, 1.23 MB

english, 2014

13

Editorial Board

Citirak, Gülsenay, Witting, Nanna, Duno, Morten, Werlauff, Ulla, Petri, Helle, Vissing, John

Journal:

Primary Care: Clinics in Office Practice

Year:

1997

Language:

english

File:

PDF, 93 KB

english, 1997

14

P.7.2 Natural history of a steroid naive DMD cohort

Steffensen, B.F., Jeppesen, J., Werlauff, U., Rahbek, J.

Journal:

Neuromuscular Disorders

Year:

2013

Language:

english

File:

PDF, 58 KB

english, 2013

15

Letter from the Royal Commission for the Preservation of Antiquities, Copenhagen

Frederik, Werlauff, Finn Magnusen, C. J. Thomsen and C. C. Rafn

Journal:

Proceedings of the Royal Irish Academy (1836-1869)

Year:

1847-1850

Language:

english

File:

PDF, 204 KB

english, 1847-1850

16

G.P.164

Werge, B., Rahbek, J., Madsen, A., Marquardt, J., Werlauff, U., Steffensen, B.F.

Journal:

Neuromuscular Disorders

Year:

2014

Language:

english

File:

PDF, 56 KB

english, 2014

17

Class Actions in Denmark

Journal:

The ANNALS of the American Academy of Political and Social Science

Year:

2009

Language:

english

File:

PDF, 44 KB

english, 2009

18

The applicability of four clinical methods to evaluate arm and hand function in all stages of spinal muscular atrophy type II

Werlauff, Ulla, Fynbo Steffensen, Birgit

Journal:

Disability & Rehabilitation

Year:

2014

Language:

english

File:

PDF, 216 KB

english, 2014

19

Development of a patient-reported outcome measure for arm and hand function in Duchenne muscular dystrophy (UL-PROM DMD)

Klingels, K., Mayhew, A., Mazzone, E., Main, M., Decostre, V., van den Hauwe, M., Eagle, M., Duong, T., de Groot, I., Ricotti, V., Werlauff, U., Campion, G., Vroom, E., Mercuri, E., Goemans, N.

Journal:

Neuromuscular Disorders

Year:

2015

Language:

english

File:

PDF, 204 KB

english, 2015

20

Health related quality of life in European adults with DMD: Results from the Care-NMD-project

Steffensen, B., Otto, C., Werlauff, U., Rahbek, J., Hoejberg, A., Kirschner, J., Vry, J., Gramsch, K.

Journal:

Neuromuscular Disorders

Year:

2015

Language:

english

File:

PDF, 203 KB

english, 2015

21

A third case of congenital myasthenic syndrome caused by mutations in SCN4A

Witting, N., Werlauff, U., Ballegaard, M., Vissing, J.

Journal:

Neuromuscular Disorders

Year:

2015

Language:

english

File:

PDF, 207 KB

english, 2015

22

Development of a patient-reported outcome measure for upper limb function in Duchenne muscular dystrophy: DMD Upper Limb PROM

Klingels, K, Mayhew, A G, Mazzone, E S, Duong, T, Decostre, V, Werlauff, U, Vroom, E, Mercuri, E, Goemans, N M

Journal:

Developmental Medicine & Child Neurology

Year:

2016

Language:

english

File:

PDF, 387 KB

english, 2016

23

Orofacial problems in patients with Duchenne muscular dystrophy and spinal muscular atrophy

Werlauff, U., Rahbek, J., Steffensen, B.

Journal:

Neuromuscular Disorders

Year:

2016

Language:

english

File:

PDF, 188 KB

english, 2016

24

Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in Denmark

Witting, Nanna, Werlauff, Ulla, Duno, Morten, Vissing, John

Journal:

Neurology: Genetics

Year:

2017

Language:

english

File:

PDF, 645 KB

english, 2017

25

Pain and fatigue in manifesting carriers of Duchenne and Becker muscular dystrophy

Drivsholm, P., Werlauff, U.

Journal:

Neuromuscular Disorders

Year:

2016

Language:

english

File:

PDF, 191 KB

english, 2016

26

Frequency and Phenotype of Myotubular Myopathy Amongst Danish Patients with Congenital Myopathy Older than 5 Years

Werlauff, U., Petri, H., Witting, N., Vissing, J.

Journal:

Journal of Neuromuscular Diseases

Year:

2015

Language:

english

File:

PDF, 259 KB

english, 2015

27

FSHD / OPMD / EDMD / DMI

Drivsholm, P., Busk, L., Nybro, T., Werlauff, U.

Journal:

Neuromuscular Disorders

Year:

2018

Language:

english

File:

PDF, 59 KB

english, 2018

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