Horacio Kaufmann is a Neurologist in New York, New York. Kaufmann has been practicing medicine for over 44 years and is rated as an Elite expert by MediFind in the treatment of Hereditary Sensory and Autonomic Neuropathy Type 2. He is also highly rated in 21 other conditions, according to our data. His top areas of expertise are Familial Dysautonomia, Hereditary Sensory and Autonomic Neuropathy Type 2, Hajdu-Cheney Syndrome, and Multiple System Atrophy. He is licensed to treat patients in New York.
Ingo Kurth practices in Jena, Germany. Kurth is rated as a Distinguished expert by MediFind in the treatment of Hereditary Sensory and Autonomic Neuropathy Type 2. He is also highly rated in 14 other conditions, according to our data. His top areas of expertise are Hereditary Sensory Neuropathy Type 1 HSN1, Congenital Insensitivity to Pain with Anhidrosis, Anhidrosis, Hereditary Sensory and Autonomic Neuropathy Type 2, and Bone Marrow Transplant.
Hanna Maayan practices in Jerusalem, Israel. Maayan is rated as a Distinguished expert by MediFind in the treatment of Hereditary Sensory and Autonomic Neuropathy Type 2. She is also highly rated in 4 other conditions, according to our data. Her top areas of expertise are Hajdu-Cheney Syndrome, Hereditary Sensory and Autonomic Neuropathy Type 2, Autonomic Neuropathy, and Familial Dysautonomia.
Summary: CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, in...
Summary: The aim of the study is to examine the validity of peripheral oxygen saturation measurement during the 6-minute walk test in patients with Systemic Sclerosis (SSc) and to examine the utility of two other functional tests as markers of pulmonary involvement in patients with SSc.
Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center