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Results of search for 'au:"Vorgerd, M"', page 1 of 3
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Authors
Burwinkel, B
Deschauer, M
Epplen, J T
Fischer, D
Gläser, D
Grehl, T
Heyer, C M
Huebner, A
Kley, R A
Kress, W
Malin, J P
Mortier, W
Ristow, M
Schröder, J M
Schröder, R
Schöls, L
Sindern, E
Tegenthoff, M
Vorgerd, M
Zange, J
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Base Sequence
Biopsy
Child
DNA Mutational Analysis
Female
Humans
Magnetic Resonance Imaging
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Middle Aged
Muscle, Skeletal
Muscular Diseases
Mutation
Mutation, Missense
diagnosis
genetics
metabolism
pathology
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English
German
Your search returned 60 results.
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1.
[Standard treatment for myositis and muscular dystrophies].
[electronic resource]
by
Schmidt, J
Vorgerd, M
Producer:
20120315
In:
Der Nervenarzt
vol. 82
Online resources:
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2.
[Metabolic and mitochondrial myopathies].
[electronic resource]
by
Vorgerd, M
Deschauer, M
Producer:
20131017
In:
Zeitschrift fur Rheumatologie
vol. 72
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3.
Treatment of glycogenosys type V (McArdle disease) with creatine and ketogenic diet with clinical scores and with 31P-MRS on working leg muscle.
[electronic resource]
by
Vorgerd, M
Zange, J
Producer:
20080206
In:
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
vol. 26
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4.
[Camptocormia in the differential diagnosis of hyperkyphosis and ankylosing spondylitis].
[electronic resource]
by
Sarholz, M
Vorgerd, M
Braun, J
Producer:
20130103
In:
Deutsche medizinische Wochenschrift (1946)
vol. 137
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5.
[Hepatitis B associated polyarteriitis nodosa with cerebral vasculitis].
[electronic resource]
by
Kohlhaas, K
Brechmann, T
Vorgerd, M
Producer:
20070910
In:
Deutsche medizinische Wochenschrift (1946)
vol. 132
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6.
[Chronic progressive external ophthalmoplegia plus: diagnosis with muscular magnetic resonance tomography].
[electronic resource]
by
Peters, S
Vorgerd, M
Heyer, C M
Producer:
20061120
In:
RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin
vol. 178
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7.
Creatine for treating muscle disorders.
[electronic resource]
by
Kley, R A
Vorgerd, M
Tarnopolsky, M A
Producer:
20070508
In:
The Cochrane database of systematic reviews
no. 1
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8.
Creatine treatment in muscle disorders: a meta-analysis of randomised controlled trials.
[electronic resource]
by
Kley, R A
Tarnopolsky, M A
Vorgerd, M
Producer:
20080407
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 79
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9.
Assessment of postexcitatory inhibition in patients with focal dystonia.
[electronic resource]
by
Schwenkreis, P
Vorgerd, M
Malin, J P
Tegenthoff, M
Producer:
19991124
In:
Acta neurologica Scandinavica
vol. 100
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10.
A missense point mutation (Ser515Phe) in the adrenoleukodystrophy gene in a family with adrenomyeloneuropathy: a clinical, biochemical, and genetic study.
[electronic resource]
by
Vorgerd, M
Fuchs, S
Tegenthoff, M
Malin, J P
Producer:
19950404
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 58
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11.
Spinal MRI in progressive myeloneuropathy associated with vitamin E deficiency.
[electronic resource]
by
Vorgerd, M
Tegenthoff, M
Kühne, D
Malin, J P
Producer:
19970115
In:
Neuroradiology
vol. 38 Suppl 1
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12.
[Nervus interosseus anterior syndrome (Kiloh-Nevin syndrome)--diagnosis with MRI].
[electronic resource]
by
Roggenland, D
Heyer, C M
Vorgerd, M
Nicolas, V
Producer:
20080717
In:
RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin
vol. 180
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13.
Deficiency of phosphofructo-1-kinase/muscle subtype in humans impairs insulin secretion and causes insulin resistance.
[electronic resource]
by
Ristow, M
Vorgerd, M
Möhlig, M
Schatz, H
Pfeiffer, A
Producer:
19980114
In:
The Journal of clinical investigation
vol. 100
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14.
Insulin resistance and impaired insulin secretion due to phosphofructo-1-kinase-deficiency in humans.
[electronic resource]
by
Ristow, M
Vorgerd, M
Möhlig, M
Schatz, H
Pfeiffer, A
Producer:
19990819
In:
Journal of molecular medicine (Berlin, Germany)
vol. 77
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15.
Idebenone in patients with Friedreich ataxia.
[electronic resource]
by
Schöls, L
Vorgerd, M
Schillings, M
Skipka, G
Zange, J
Producer:
20010802
In:
Neuroscience letters
vol. 306
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16.
Postexcitatory inhibition after transcranial magnetic single and double brain stimulation in Huntington's disease.
[electronic resource]
by
Tegenthoff, M
Vorgerd, M
Juskowiak, F
Roos, V
Malin, J P
Producer:
19961022
In:
Electroencephalography and clinical neurophysiology
vol. 101
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17.
Adult-onset glycogen storage disease type II: phenotypic and allelic heterogeneity in German patients.
[electronic resource]
by
Vorgerd, M
Burwinkel, B
Reichmann, H
Malin, J P
Kilimann, M W
Producer:
20000413
In:
Neurogenetics
vol. 1
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18.
Mitochondrial impairment of human muscle in Friedreich ataxia in vivo.
[electronic resource]
by
Vorgerd, M
Schöls, L
Hardt, C
Ristow, M
Epplen, J T
Zange, J
Producer:
20000915
In:
Neuromuscular disorders : NMD
vol. 10
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19.
[Adrenoleukodystrophy and adrenomyeloneuropathy. Clinical biochemical and molecular genetic findings].
[electronic resource]
by
Vorgerd, M
Benkmann, H G
Tegenthoff, M
Gal, A
Malin, J P
Producer:
19980604
In:
Der Nervenarzt
vol. 69
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20.
Polymyositis of the skeletal muscles as an extraintestinal complication in quiescent ulcerative colitis.
[electronic resource]
by
Voigt, E
Griga, T
Tromm, A
Henschel, M G
Vorgerd, M
May, B
Producer:
20000321
In:
International journal of colorectal disease
vol. 14
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