Vorgerd M - Search Results

1

Heterozygous expansion of the GAA tract of the X25/frataxin gene is associated with insulin resistance in humans.

Hebinck J, Hardt C, Schöls L, Vorgerd M, Briedigkeit L, Kahn CR, Ristow M. Hebinck J, et al. Among authors: vorgerd m. Diabetes. 2000 Sep;49(9):1604-7. doi: 10.2337/diabetes.49.9.1604. Diabetes. 2000. PMID: 10969848

2

Muscle phosphofructokinase deficiency in two generations.

Vorgerd M, Karitzky J, Ristow M, Van Schaftingen E, Tegenthoff M, Jerusalem F, Malin JP. Vorgerd M, et al. J Neurol Sci. 1996 Sep 15;141(1-2):95-9. doi: 10.1016/0022-510x(96)00131-1. J Neurol Sci. 1996. PMID: 8880699

3

Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.

Schöls L, Gispert S, Vorgerd M, Menezes Vieira-Saecker AM, Blanke P, Auburger G, Amoiridis G, Meves S, Epplen JT, Przuntek H, Pulst SM, Riess O. Schöls L, et al. Among authors: vorgerd m. Arch Neurol. 1997 Sep;54(9):1073-80. doi: 10.1001/archneur.1997.00550210011007. Arch Neurol. 1997. PMID: 9311350

4

Deficiency of phosphofructo-1-kinase/muscle subtype in humans impairs insulin secretion and causes insulin resistance.

Ristow M, Vorgerd M, Möhlig M, Schatz H, Pfeiffer A. Ristow M, et al. Among authors: vorgerd m. J Clin Invest. 1997 Dec 1;100(11):2833-41. doi: 10.1172/JCI119831. J Clin Invest. 1997. PMID: 9389749 Free PMC article.

5

An association between NIDDM and a GAA trinucleotide repeat polymorphism in the X25/frataxin (Friedreich's ataxia) gene.

Ristow M, Giannakidou E, Hebinck J, Busch K, Vorgerd M, Kotzka J, Knebel B, Mueller-Berghaus J, Epplen C, Pfeiffer A, Kahn CR, Doria A, Krone W, Mueller-Wieland D. Ristow M, et al. Among authors: vorgerd m. Diabetes. 1998 May;47(5):851-4. doi: 10.2337/diabetes.47.5.851. Diabetes. 1998. PMID: 9588463

6

Insulin resistance and impaired insulin secretion due to phosphofructo-1-kinase-deficiency in humans.

Ristow M, Vorgerd M, Möhlig M, Schatz H, Pfeiffer A. Ristow M, et al. Among authors: vorgerd m. J Mol Med (Berl). 1999 Jan;77(1):96-103. doi: 10.1007/s001090050311. J Mol Med (Berl). 1999. PMID: 9930938

7

Deficiency of phosphofructo-1-kinase/muscle subtype in humans is associated with impairment of insulin secretory oscillations.

Ristow M, Carlqvist H, Hebinck J, Vorgerd M, Krone W, Pfeiffer A, Müller-Wieland D, Ostenson CG. Ristow M, et al. Among authors: vorgerd m. Diabetes. 1999 Aug;48(8):1557-61. doi: 10.2337/diabetes.48.8.1557. Diabetes. 1999. PMID: 10426373

8

Mitochondrial impairment of human muscle in Friedreich ataxia in vivo.

Vorgerd M, Schöls L, Hardt C, Ristow M, Epplen JT, Zange J. Vorgerd M, et al. Neuromuscul Disord. 2000 Aug;10(6):430-5. doi: 10.1016/s0960-8966(00)00108-5. Neuromuscul Disord. 2000. PMID: 10899450 Clinical Trial.

9

Oxidative stress in patients with Friedreich ataxia.

Schulz JB, Dehmer T, Schöls L, Mende H, Hardt C, Vorgerd M, Bürk K, Matson W, Dichgans J, Beal MF, Bogdanov MB. Schulz JB, et al. Among authors: vorgerd m. Neurology. 2000 Dec 12;55(11):1719-21. doi: 10.1212/wnl.55.11.1719. Neurology. 2000. PMID: 11113228

10

Idebenone in patients with Friedreich ataxia.

Schöls L, Vorgerd M, Schillings M, Skipka G, Zange J. Schöls L, et al. Among authors: vorgerd m. Neurosci Lett. 2001 Jun 29;306(3):169-72. doi: 10.1016/s0304-3940(01)01892-4. Neurosci Lett. 2001. PMID: 11406322 Clinical Trial.

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