Publikationen 2002

  • What's in the serum of seronegative MG and LEMS?: MuSK et al. (Neurology)
    Abicht A, Lochmüller H
  • Creatine monohydrate in myotonic dystrophy: a double-blind, placebo-controlled clinical study. (J Neurol)
    Walter MC, Reilich P, Lochmüller H, Kohnen R, Schlotter B, Hautmann H, Dunkl E, Pongratz D, Müller-Felber W
  • De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy. (Neuromuscul Disord)
    Durling HJ, Reilich P, Müller-Höcker J, Mendel B, Pongratz D, Wallgren-Pettersson C, Gunning P, Lochmüller H, Laing NG
  • [Polyneuropathy--treatment] (Dtsch Med Wochenschr)
    Schlotter-Weigel B, Pongratz DE
  • [Polyneuropathy--diagnostic] (Dtsch Med Wochenschr)
    Schlotter-Weigel B, Pongratz DE
  • [Polyneuropathy--Case report] (Dtsch Med Wochenschr)
    Schlotter-Weigel B, Pongratz DE
  • Congenital myasthenic syndrome (CMS) in three European kinships due to a novel splice mutation (IVS7 - 2 A/G) in the epsilon acetylcholine receptor (AChR) subunit gene. (Neuropediatrics)
    Barisic N, Schmidt C, Sidorova OP, Herczegfalvi A, Gekht BM, Song IH, Stucka R, Karcagi V, Abicht A, Lochmüller H
  • [26-year-old female patient with elevated liver enzymes] (Z Gastroenterol)
    Martin K, Schlotter B, Müller-Höcker J, Loeschke K, Pongratz D, Folwaczny C
  • A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population. (Neuromuscul Disord)
    Gross M, Rötzer E, Kölle P, Mortier W, Reichmann H, Goebel HH, Lochmüller H, Pongratz D, Mahnke-Zizelman DK, Sabina RL
  • [Fistula Banding - Success-promoting Approach in Peripheral Steal Syndrome] (Zentralbl Chir)
    Meyer F, Müller JS, Grote R, Halloul Z, Lippert H, Bürger T
  • [Pneumoperitoneum as occasional finding in chronic dialysis patients--laparotomy or conservative non-operative approach?] (Zentralbl Chir)
    Meyer F, Müller JS, Lippert H
  • A newly identified chromosomal microdeletion and an N-box mutation of the AChR epsilon gene cause a congenital myasthenic syndrome. (Brain)
    Abicht A, Stucka R, Schmidt C, Briguet A, Höpfner S, Song IH, Pongratz D, Müller-Felber W, Ruegg MA, Lochmüller H
  • [Intestinal pseudoobstructions and gastric necrosis in mitochondrial myopathy] (Dtsch Med Wochenschr)
    Muehlenberg K, Fiedler A, Schaumann I, Müller-Felber W, Wiedmann KH
  • [Experiences with ambulatory arteriovenous shunt surgery. A cost-benefit analysis] (Chirurg)
    Meyer F, Müller JS, Bürger T, Halloul Z, Lippert H
  • Acute effects of maternal smoking on fetal-placental-maternal system hemodynamics. (Arq Bras Cardiol)
    Müller JS, Antunes M, Behle I, Teixeira L, Zielinsky P
  • Depletion of mitochondrial DNA in the liver of an infant with neonatal giant cell hepatitis. (Hum Pathol)
    Müller-Höcker J, Muntau A, Schäfer S, Jaksch M, Staudt F, Pongratz D, Taanman JW
  • Screening for carnitine palmitoyltransferase II deficiency by tandem mass spectrometry. (J Inherit Metab Dis)
    Gempel K, Kiechl S, Hofmann S, Lochmüller H, Kiechl-Kohlendorfer U, Willeit J, Sperl W, Rettinger A, Bieger I, Pongratz D, Gerbitz KD, Bauer MF
  • Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromes. (Neurology)
    Merlini L, Gooding R, Lochmüller H, Müller-Felber W, Walter MC, Angelicheva D, Talim B, Hallmayer J, Kalaydjieva L