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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Agnosia[original query]
Posterior cortical atrophy as an extreme phenotype of GRN mutations.
JAMA neurology 2014 12 72 (2): 224-8.
Caroppo Paola, Belin Catherine, Grabli David, Maillet Didier, De Septenville Anne, Migliaccio Raffaella, Clot Fabienne, Lamari Foudil, Camuzat Agnès, Brice Alexis, Dubois Bruno, Le Ber Isabel
An autopsy case of type A FTLD-TDP with a GRN mutation presenting with the logopenic variant of primary progressive aphasia at onset and with corticobasal syndrome subsequently.
Neuropathology : official journal of the Japanese Society of Neuropathology 2024 5 .
Takafumi Tomenaga, Shinobu Minatani, Hiroto Namba, Akitoshi Takeda, Takahito Yoshizaki, Joji Kawabe, Nazere Keyoumu, Hiroyuki Morino, Makoto Higuchi, Tomoyasu Matsubara, Hiroyuki Hatsuta, Masato Hasegawa, Shigeo Murayama, Yoshiaki It
Posterior Cortical Atrophy Due to Alzheimer Disease in a Person With Down Syndrome: A Case Report.
Neurology 2024 12 104 (1): e210179.
Íñigo Rodríguez-Baz, Bessy Benejam, Alejandra O Morcillo-Nieto, Lídia Vaqué-Alcázar, José Enrique Arriola-Infante, Valle Camacho, Mateus Rozalem Aranha, Maria Carmona-Iragui, Laura Videla, Isabel Barroeta, Susana Fernández, Sara E Zsadanyi, Sandra Giménez, Javier Arranz, Lucia Maure Blesa, Daniel Alcolea, Alberto Lleó, Alexandre Bejanin, Juan Fort
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