Kennedy's disease, also known as bulbospinal muscular atrophy (BSMA), is a rare, adult-
onset, X-linked, recessive trinucleotide, polyglutamine (poly-G) disorder, caused by …

Bulbar and spinal muscular atrophy (BSMA) is an adult‐onset, X‐linked recessive
trinucleotide, polyglutamine disorder, caused by expansion of a polymorphic CAG tandem …

We review the genetic and clinical features of spinobulbar muscular atrophy (SBMA), a
progressive neuromuscular disorder caused by a CAG/glutamine tract expansion in the …

Purpose Spinal and bulbar muscular atrophy (SBMA) is an X-linked motor neuron disease
characterized by proximal muscle weakness, muscle atrophy, and fasciculation. Although …

Supplement 10_07-08-2021_OrphanAnesthesia.indd Page 1 O ffizielles Organ: Deutsche
Gesellschaft für Anästhesiologie und Intensivmedizin eV (DGAI) Berufsverband Deutscher …

The article discusses the anaesthesia recommendations for Kennedy disease (KD), which is
an adult-onset, X-linked recessive trinucleotide, polyglutamine (poly-G) disorder. Symptoms …

Spinobulbar muscular atrophy (SBMA), or Kennedy's disease, is an inherited neuromuscular
disorder caused by a polyglutamine (polyQ) tract expansion in the androgen receptor (AR) …

The anabolic steroid hormones are of key importance in the integrated control of metabolic
homeostasis and sexual differentiation. Since their initial discovery in the 1930s, the …

The polyglutamine diseases are a clinically heterogeneous group of inherited
neurodegenerative disorders caused by expansion of polyglutamine-encoding (CAG) n …

Once again, the field of neuromuscular diseases has produced a wide-ranging and
interesting group of papers, a small number of which are highlighted. Many papers focus on …