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Analysis of COL7A1 pathogenic variants in a large cohort of dystrophic epidermolysis bullosa patients from Argentina reveals a new genotype-phenotype correlation.
Am J Med Genet A. 2022 Nov;188(11):3153-3161. doi: 10.1002/ajmg.a.62957. Epub 2022 Aug 18.
Am J Med Genet A. 2022.
PMID: 35979658
A novel pathogenic FERMT1 variant in four families with Kindler syndrome in Argentina.
Valinotto LE, Natale MI, Lusso SB, Cella E, Gutiérrez O, Sebastiani F, Manzur GB.
Valinotto LE, et al. Among authors: manzur gb.
Pediatr Dermatol. 2020 Mar;37(2):337-341. doi: 10.1111/pde.14076. Epub 2020 Jan 20.
Pediatr Dermatol. 2020.
PMID: 31957900
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Ichthyosis follicularis, atrichia and photophobia (IFAP) and hereditary mucoepithelial dysplasia: Two syndromes that share a common clinical spectrum.
Irurzun I, Natale MI, Agostinelli ML, Lamberti M, Montero D, Granda C, Mássimo JA, Manzur GB, Valinotto LE.
Irurzun I, et al. Among authors: manzur gb.
Pediatr Dermatol. 2021 May;38(3):568-574. doi: 10.1111/pde.14560. Epub 2021 Mar 19.
Pediatr Dermatol. 2021.
PMID: 33742461
Review.
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Self-help epilepsy groups: an evaluation of effect on depression and schizophrenia.
Becú M, Becú N, Manzur G, Kochen S.
Becú M, et al.
Epilepsia. 1993 Sep-Oct;34(5):841-5. doi: 10.1111/j.1528-1157.1993.tb02100.x.
Epilepsia. 1993.
PMID: 8404735
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