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searching for Familial Amyloidosis, Finnish Type 4 found (7 total)

alternate case: familial Amyloidosis, Finnish Type

Ardalan–Shoja–Kiuru syndrome (238 words) [view diff] case mismatch in snippet view article find links to article

ophthalmologist Jouko Meretoja and is known as Meretoja syndrome or Familial Amyloidosis, Finnish type. In addition to the classic manifestations of Finnish type

Cerebral amyloid angiopathy (1,768 words) [view diff] no match in snippet view article find links to article

respectively. Both peptides are linked to mutations in ITM2B. Familial amyloidosis-Finnish type is associated with gelsolin amyloid (AGel). The vascular amyloid

Amyloid (6,516 words) [view diff] case mismatch in snippet view article find links to article

C-III ApoCIII amyloidosis AApoCIII fragments of Gelsolin Familial amyloidosis, Finnish type AGel Lysozyme Hereditary non-neuropathic systemic amyloidosis

Plasma gelsolin (9,144 words) [view diff] no match in snippet view article find links to article

Robert C. (2019-07-09). "The role of gelsolin domain 3 in familial amyloidosis (Finnish type)". Proceedings of the National Academy of Sciences. 116 (28):