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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1984 1
1995 2
1996 1
1999 4
2006 1
2008 1
2012 1
2013 2
2014 2
2021 2
2022 0
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15 results
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Page 1
Corrigendum: Case Report: Two Monochorionic Twins With a Critically Different Course of Progressive Osseous Heteroplasia.
Justicia-Grande AJ, Gómez-Ríal J, Rivero-Calle I, Pischedda S, Curras-Tuala MJ, Gómez-Carballa A, Cebey-López M, Pardo-Seco J, Méndez-Gallart R, Fernández-Seara MJ, Salas A, Martinón-Torres F. Justicia-Grande AJ, et al. Among authors: fernandez seara mj. Front Pediatr. 2021 Dec 14;9:807812. doi: 10.3389/fped.2021.807812. eCollection 2021. Front Pediatr. 2021. PMID: 34970520 Free PMC article.
Case Report: Two Monochorionic Twins With a Critically Different Course of Progressive Osseus Heteroplasia.
Justicia-Grande AJ, Gómez-Ríal J, Rivero-Calle I, Pischedda S, Curras-Tuala MJ, Gómez-Carballa A, Cebey-López M, Pardo-Seco J, Méndez-Gallart R, Fernández-Seara MJ, Salas A, Martinón-Torres F. Justicia-Grande AJ, et al. Among authors: fernandez seara mj. Front Pediatr. 2021 Jun 23;9:662669. doi: 10.3389/fped.2021.662669. eCollection 2021. Front Pediatr. 2021. PMID: 34249809 Free PMC article.
[Partial trisomy of chromosome 5p].
Marcos Alonso S, Carreira Sande N, Couce Pico ML, Fernández Seara MJ, Fernández Bouzas R, Martínez Yriarte JM. Marcos Alonso S, et al. Among authors: fernandez seara mj. An Pediatr (Barc). 2006 Feb;64(2):185-6. doi: 10.1157/13084190. An Pediatr (Barc). 2006. PMID: 16527083 Free article. Spanish. No abstract available.
Peutz-Jeghers syndrome in a neonate.
Fernandez Seara MJ, Martinez Soto MI, Fernandez Lorenzo JR, Trabazo S, Gamborino E, Forteza Vila J. Fernandez Seara MJ, et al. J Pediatr. 1995 Jun;126(6):965-7. doi: 10.1016/s0022-3476(95)70224-5. J Pediatr. 1995. PMID: 7776109
[Congenital chloridorrhea: adjuvant therapy with ibuprofen and ranitidine].
Martinón-Torres F, Fernández Seara MJ, del Río Pastoriza I, Rodrigo Sáez E, Martinón Sánchez JM, Castro-Gago M. Martinón-Torres F, et al. Among authors: fernandez seara mj. An Esp Pediatr. 1999 Jun;50(6):619-22. An Esp Pediatr. 1999. PMID: 10410429 Review. Spanish. No abstract available.
[Oculocutaneous albinism 1B associated with a new mutation in the TYR gene].
Vidal-Ríos P, Fernández-Seara MJ, Cortés E, Hurtado L, Couce ML. Vidal-Ríos P, et al. Among authors: fernandez seara mj. An Pediatr (Barc). 2013 May;78(5):339-40. doi: 10.1016/j.anpedi.2012.09.006. Epub 2012 Oct 22. An Pediatr (Barc). 2013. PMID: 23085315 Free article. Spanish. No abstract available.
15 results