|1.||Suter, Ueli: 3 articles (03/2014 - 09/2005)|
|2.||Niemann, Axel: 3 articles (03/2014 - 09/2005)|
|3.||Huber, Nina: 2 articles (03/2014 - 05/2011)|
|4.||Chumillas, María José: 2 articles (11/2008 - 09/2003)|
|5.||Sevilla, Teresa: 2 articles (11/2008 - 09/2003)|
|6.||Palau, Francesc: 2 articles (11/2008 - 09/2003)|
|7.||Horn, Michael: 1 article (03/2014)|
|8.||Feltri, M Laura: 1 article (03/2014)|
|9.||Wagner, Konstanze M: 1 article (03/2014)|
|10.||Angst, Brigitte: 1 article (03/2014)|
|1.||Charcot-Marie-Tooth Disease (Peroneal Muscular Atrophy)
03/01/2014 - "The ganglioside-induced differentiation-associated protein 1 (GDAP1) is a mitochondrial fission factor and mutations in GDAP1 cause Charcot-Marie-Tooth disease. "
05/01/2011 - "Charcot-Marie-Tooth disease (CMT) caused by mutations in the ganglioside-induced differentiation-associated protein 1 (GDAP1) gene is characterized by a spectrum of phenotypes. "
01/01/2008 - "A wide range of phenotypes have been reported in autosomal recessive (AR) Charcot-Marie-Tooth disease (CMT) patients carrying mutations in the ganglioside-induced differentiation-associated protein 1 (GDAP1) gene, such as axonal, demyelinating, and intermediate forms of AR CMT. "
09/26/2005 - "Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease."
11/01/2003 - "Based on the electrophysiological tests, patients with ganglioside-induced differentiation-associated protein 1 mutations will therefore be classified as either axonal or demyelinating Charcot-Marie-Tooth disease. "
|2.||Vocal Cord Paralysis
12/24/2002 - "Mutations in the ganglioside-induced differentiation-associated protein 1 gene (GDAP1) were recently shown to be responsible for autosomal recessive (AR) demyelinating Charcot-Marie-Tooth disease (CMT) type 4A (CMT4A) as well as AR axonal CMT with vocal cord paralysis. "
11/01/2003 - "Mutations in the ganglioside-induced differentiation-associated protein 1 gene cause either autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4A or autosomal recessive axonal Charcot-Marie-Tooth disease with vocal cord paresis. "
|3.||Severe Acute Respiratory Syndrome
01/09/2009 - "We have here characterized three novel human macro domain proteins that were found to reside either in the cytoplasm and nucleus [macro domain protein 2 (MDO2) and ganglioside-induced differentiation-associated protein 2] or in mitochondria [macro domain protein 1 (MDO1)], and compared them with viral macro domains from Semliki Forest virus, hepatitis E virus, and severe acute respiratory syndrome coronavirus, and with a yeast macro protein, Poa1p. "
|4.||Mitochondrial Diseases (Mitochondrial Disease)
12/01/2012 - "Neuropathies were first reported in diseases related to point mutations of mitochondrial DNA, but they proved to be a prominent feature of the phenotype in mitochondrial disorders caused by defects in nuclear DNA, particularly in 3 genes: polymerase gamma 1 (POLG1), mitofusin 2 (MFN2), and ganglioside-induced differentiation-associated protein 1 (GDAP1). "
|5.||Hereditary Sensory and Motor Neuropathy (Dejerine Sottas Disease)
|1.||Proteins (Proteins, Gene)
|3.||Staphylococcal Protein A (A, Protein)
|4.||Phosphopyruvate Hydratase (Enolase)
|5.||Phosphoglycerate Kinase (Kinase, Phosphoglycerate)
|6.||Heat-Shock Proteins (Heat-Shock Protein)
|7.||Mitochondrial DNA (mtDNA)
|8.||DNA (Deoxyribonucleic Acid)
|10.||Adenosine Triphosphate (ATP)