Frank Rutsch
Muenster, NW, Germany
Last Updated: 09/26/2026
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Found 104 publications
Efficacy and safety of sepiapterin versus sapropterin in patients with phenylketonuria: Results from the Phase 3, randomized, crossover, open-label, active-controlled AMPLIPHY trial.
Journal: Metabolism: clinical and experimental
Published: October 28, 2025
A randomized Phase 1b trial evaluating the pharmacodynamics of ilofotase alfa in adults with hypophosphatasia.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: August 14, 2025
Risk of inadequate protein and micronutrient intakes in patients with PKU with an increased phe-tolerance: Impact of a micronutrient-dense protein substitute.
Journal: Molecular genetics and metabolism reports
Published: August 06, 2025
Effect of long-term sepiapterin treatment on dietary phenylalanine tolerance in patients with phenylketonuria: Interim results from the phase 3 APHENITY Extension Study.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 01, 2025
Reduced Descending Itch Inhibition in Peripheral Neuropathy Patients With Chronic Pruritus.
Journal: European journal of pain (London, England)
Published: July 15, 2025
Effects of dietary management for medium-chain acyl-CoA dehydrogenase deficiency (MCADD) on eating behaviour in childhood, adolescence and young adulthood.
Journal: BMC nutrition
Published: May 30, 2025
Autosomal recessive hypophosphatemic rickets type 2 (ARHR2): Is phosphate supplementation safe?
Journal: Bone
Published: April 16, 2025
Long-Term Efficacy and Tolerability of Pegzilarginase in Arginase 1 Deficiency: Results of Two International Multicentre Open-Label Extension Studies.
Journal: Journal of inherited metabolic disease
Published: March 30, 2025
Necrolytic migratory erythema following prolonged continuous subcutaneous dasiglucagon administration: a rare dermatologic adverse event.
Journal: Endocrinology, diabetes & metabolism case reports
Published: January 10, 2025
Phenotypic characterization of ENPP1 deficiency: generalized arterial calcification of infancy and autosomal recessive hypophosphatemic rickets type 2.
Journal: JBMR plus
Published: November 07, 2024
Homozygous splice-site variant in ENPP1 underlies generalized arterial calcification of infancy.
Journal: BMC pediatrics
Published: August 23, 2024
Mental disorders in people with undiagnosed diseases presenting to German centres for rare diseases - prevalence, type and relevance.
Journal: Psychiatry research
Published: July 17, 2024
Last Updated: 09/26/2026