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185 Familial hemiplegic migraine Familial hemiplegic migraine FHM type 2, clinically manifested as migraine with aura, is linked to loss-of function mutations of the ATP1A2 gene encoding the astrocyte-specific 2 subunit of Na + /K + ATPase (NKA)

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Studien zeigen, dass BPC 157 die Heilung von Sehnenverletzungen frdert und dabei eine erhhte Anzahl von Fibroblasten im betroffenen Gewebe festgestellt wurde

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