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Author/Creator Gatt, Miriam

1. A multi‐country study of prevalence and early childhood mortality among children with omphalocele. Issue 20 (17th October 2020)

Authors:
Nembhard, Wendy N.; Bergman, Jorieke E. H.; Politis, Maria D.; Arteaga‐Vázquez, Jazmín; Bermejo‐Sánchez, Eva; Canfield, Mark A.; Cragan, Janet D.; Dastgiri, Saeed; de Walle, Hermien E. K.; Feldkamp, Marcia L.; Nance, Amy; Gatt, Miriam; Groisman, Boris; Hurtado‐Villa, Paula; Kallén, Kärin; Landau,...
Journal:
Birth defects research
Issue:
Volume 112:Issue 20(2020)
Page Start:
1787
Record Type:
Journal Article
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5. Amniotic band syndrome and limb body wall complex in Europe 1980–2019. Issue 4 (30th December 2022)

Authors:
Bergman, Jorieke E. H.; Barišić, Ingeborg; Addor, Marie‐Claude; Braz, Paula; Cavero‐Carbonell, Clara; Draper, Elizabeth S.; Echevarría‐González‐de‐Garibay, Luis J.; Gatt, Miriam; Haeusler, Martin; Khoshnood, Babak; Klungsøyr, Kari; Kurinczuk, Jennifer J.; Latos‐Bielenska, Anna; Luyt, Karen; Marti...
Journal:
American journal of medical genetics
Issue:
Volume 191:Issue 4(2023)
Page Start:
995
Record Type:
Journal Article
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6. Analysis of early neonatal case fatality rate among newborns with congenital hydrocephalus, a 2000–2014 multi‐country registry‐based study. Issue 12 (28th May 2022)

Authors:
Gili, Juan Antonio; López‐Camelo, Jorge Santiago; Nembhard, Wendy N.; Bakker, Marian; de Walle, Hermien E. K.; Stallings, Erin B.; Kancherla, Vijaya; Contiero, Paolo; Dastgiri, Saeed; Feldkamp, Marcia L.; Nance, Amy; Gatt, Miriam; Martínez, Laura; Canessa, María Aurora; Groisman, Boris; Hurtado‐V...
Journal:
Birth defects research
Issue:
Volume 114:Issue 12(2022)
Page Start:
631
Record Type:
Journal Article
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7. Analysis of Mortality among Neonates and Children with Spina Bifida: An International Registry‐Based Study, 2001‐2012. Issue 6 (21st October 2019)

Authors:
Bakker, Marian K.; Kancherla, Vijaya; Canfield, Mark A.; Bermejo‐Sanchez, Eva; Cragan, Janet D.; Dastgiri, Saeed; De Walle, Hermien E. K.; Feldkamp, Marcia L.; Groisman, Boris; Gatt, Miriam; Hurtado‐Villa, Paula; Kallen, Karin; Landau, Daniella; Lelong, Nathalie; Lopez Camelo, Jorge S.; Martínez,...
Journal:
Paediatric and perinatal epidemiology
Issue:
Volume 33:Issue 6(2019:Nov.)
Page Start:
436
Record Type:
Journal Article
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9. Congenital anomalies associated with trisomy 18 or trisomy 13: A registry‐based study in 16 european countries, 2000–2011. (8th September 2015)

Authors:
Springett, Anna; Wellesley, Diana; Greenlees, Ruth; Loane, Maria; Addor, Marie‐Claude; Arriola, Larraitz; Bergman, Jorieke; Cavero‐Carbonell, Clara; Csaky‐Szunyogh, Melinda; Draper, Elizabeth S.; Garne, Ester; Gatt, Miriam; Haeusler, Martin; Khoshnood, Babak; Klungsoyr, Kari; Lynch, Catherine; Di...
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 12(2015:Dec.)
Page Start:
3062
Record Type:
Journal Article
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10. Congenital clubfoot in Europe: A population‐based study. Issue 4 (10th February 2019)

Authors:
Wang, Hao; Barisic, Ingeborg; Loane, Maria; Addor, Marie‐Claude; Bailey, Linda M.; Gatt, Miriam; Klungsoyr, Kari; Mokoroa, Olatz; Nelen, Vera; Neville, Amanda J.; O'Mahony, Mary; Pierini, Anna; Rissmann, Anke; Verellen‐Dumoulin, Christine; de Walle, Hermien E.K.; Wiesel, Awi; Wisniewska, Katarzyn...
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 4(2019)
Page Start:
595
Record Type:
Journal Article
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