B. Schlotter

发表

Creatine monohydrate in myotonic dystrophy

H. Hautmann, H. Lochmüller, D. Pongratz, 2002, Journal of Neurology.

Discrepant results for cardiac troponin T and troponin I in chronic myopathy, depending on instrument and assay generation.

D. Pongratz, W. Vogt, B. Schlotter, 1996, Clinical chemistry.

Location matters – Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2P

P. Reilich, B. Hotter, F. Montagnese, 2020, Neuromuscular Disorders.

Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations

Jacqueline Palace, K. Bushby, F. Muntoni, 2012, Journal of Neurology.

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

M. Pericak-Vance, W. Hung, T. Siddique, 1998, Neurogenetics.

Creatine monohydrate in myotonic dystrophy: a double-blind, placebo-controlled clinical study.

H. Hautmann, Hanns Lochmüller, D. Pongratz, 2002, Journal of neurology.

in Chronic Myopathy, Depending on Instrument and Assay

D. Pongratz, B. Schlotter, S. Liem, 1996 .

A common mutation (ε1267delG) in congenital myasthenic patients of Gypsy ethnic origin

H. Lochmüller, R. Horvath, V. Ramaekers, 1999 .

Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect.

T. Strom, K. Bushby, Jacqueline A Palace, 2011, American journal of human genetics.

Mutation screening of the N‐myc downstream‐regulated gene 1 (NDRG1) in patients with Charcot‐Marie‐Tooth Disease

Hanns Lochmüller, Thomas Voit, P K Thomas, 2003, Human mutation.

Calf enlargement in neuromuscular diseases: a quantitative ultrasound study in 350 patients and review of the literature

C. Reimers, B. Eicke, B. Schlotter, 1996, Journal of the Neurological Sciences.

High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study

M. Toepfer, Hanns Lochmüller, H. Lochmüller, 2000, Journal of Neurology.

A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin.

Hanns Lochmüller, R. Horvath, V. Ramaekers, 1999, Neurology.

Phenotypic variability in two brothers with sarcotubular myopathy

D. Pongratz, U. Ketelsen, J. Müller‐Höcker, 1999, Journal of Neurology.

[New insights in pathogenesis and therapy of sporadic inclusion body myositis (s-IBM)].

Hanns Lochmüller, D. Pongratz, M. Walter, 2001, Der Nervenarzt.

[Effect of muscular work on the myosonogram].

Hanns Lochmüller, C. Reimers, B. Schlotter, 2008, Ultraschall in der Medizin.

Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations

Jacqueline Palace, K. Bushby, F. Muntoni, 2012, Journal of Neurology.

Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations Velina GuergueltchevaJuliane S. MullerMarina DuslJan SenderekAnders Oldfors • Christopher LindberghSusan MaxwellJaume ColomerCecilia Jimenez MallebreraAndres Nascimento • Juan J. VilchezNuria MuelasJanbernd KirschnerSha

K. Bushby, J. Senderek, M. Dusl, 2012 .