Ana Berta da Fonseca Vieira Álvares e Sousa Ferrand de Almeida
AuthID: R-002-8QK
21
TITLE: VARS2-linked mitochondrial disease - an emerging phenotypic spectrum
AUTHORS: Gouveia, Raquel; Rodrigues, Marcia; Moldovan, Oana; Sousa, Ana Berta;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
AUTHORS: Gouveia, Raquel; Rodrigues, Marcia; Moldovan, Oana; Sousa, Ana Berta;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
INDEXED IN: 
WOS
WOS22
TITLE: Looking beyond mitral valve prolapse and ischaemic stroke - a late diagnosis of trichorhinophalangeal syndrome type I
AUTHORS: Soares, Marta P.; Rodrigues, Marcia; Silva, Daniela P.; Melo, Teresa Pinho; Sousa, Ana Berta;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
AUTHORS: Soares, Marta P.; Rodrigues, Marcia; Silva, Daniela P.; Melo, Teresa Pinho; Sousa, Ana Berta;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
INDEXED IN: WOS
WOS23
TITLE: Looking back on copy gains: a retrospective review of clinical relevance and structural mechanisms
AUTHORS: Custodio, Sonia; Silveira Santos, Rosario; Rodrigues, Raquel; Rolo, Eva; Dupont, Juliette; Dias, Patricia; Moldovan, Oana; Machado, Catarina; Rodrigues, Marcia; Sa, Mariana Soeiro; Travessa, Andre; Alves, Joao Rodrigues; Silva, Raquel Gouveia; Sousa, Ana Berta; Sousa, Ana;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
AUTHORS: Custodio, Sonia; Silveira Santos, Rosario; Rodrigues, Raquel; Rolo, Eva; Dupont, Juliette; Dias, Patricia; Moldovan, Oana; Machado, Catarina; Rodrigues, Marcia; Sa, Mariana Soeiro; Travessa, Andre; Alves, Joao Rodrigues; Silva, Raquel Gouveia; Sousa, Ana Berta; Sousa, Ana;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
INDEXED IN: WOS
WOS24
TITLE: Sixth family with confirmed metaphyseal dysplasia, Spahr type and a novel variant in MMP13: case report and review of the literature
AUTHORS: Travessa, Andre M.; Modamio Hoybjor, Silvia; Heath, Karen E.; Sousa, Ana Berta;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
AUTHORS: Travessa, Andre M.; Modamio Hoybjor, Silvia; Heath, Karen E.; Sousa, Ana Berta;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
INDEXED IN: WOS
WOS25
TITLE: The Added Value of a Multidisciplinary Clinic for Systemic Autoinflammatory Diseases
AUTHORS: Zinterl, Carolina; Costa Reis, Patricia; Esteves, Isabel Castro; Marques, Jose Goncalo; Sousa, Ana Berta; Fonseca, Joao Eurico; Ramos, Filipa Oliveira;
PUBLISHED: 2022, SOURCE: JOURNAL OF MULTIDISCIPLINARY HEALTHCARE, VOLUME: 15
AUTHORS: Zinterl, Carolina; Costa Reis, Patricia; Esteves, Isabel Castro; Marques, Jose Goncalo; Sousa, Ana Berta; Fonseca, Joao Eurico; Ramos, Filipa Oliveira;
PUBLISHED: 2022, SOURCE: JOURNAL OF MULTIDISCIPLINARY HEALTHCARE, VOLUME: 15
26
TITLE: Face-sparing Congenital Generalized Lipodystrophy Type 1 Associated With Nonclassical Congenital Adrenal Hyperplasia
AUTHORS: Costa, Sara; Sampaio, Lurdes; Berta Sousa, Ana; Xing, Chao; Agarwal, Anil K.; Garg, Abhimanyu;
PUBLISHED: 2022, SOURCE: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, VOLUME: 107, ISSUE: 9
AUTHORS: Costa, Sara; Sampaio, Lurdes; Berta Sousa, Ana; Xing, Chao; Agarwal, Anil K.; Garg, Abhimanyu;
PUBLISHED: 2022, SOURCE: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, VOLUME: 107, ISSUE: 9
27
TITLE: Anisometropia and asymmetric ABCA4-related cone-rod dystrophy
AUTHORS: Santos, Cristina; Almeida, Andreia; Pinto, Rita; Kaminska, Karolina; Peter, Virginie G.; Sousa, Ana Berta; Rivolta, Carlo; Coutinho Santos, Luisa;
PUBLISHED: 2022, SOURCE: OPHTHALMIC GENETICS, VOLUME: 43, ISSUE: 4
AUTHORS: Santos, Cristina; Almeida, Andreia; Pinto, Rita; Kaminska, Karolina; Peter, Virginie G.; Sousa, Ana Berta; Rivolta, Carlo; Coutinho Santos, Luisa;
PUBLISHED: 2022, SOURCE: OPHTHALMIC GENETICS, VOLUME: 43, ISSUE: 4
28
TITLE: EXPANDING THE CLINICAL SPECTRUM OF COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY ASSOCIATED WITH MRPS34 GENE: A MILD CASE WITH SLENDER HABITUS Full Text
AUTHORS: Ramos Travessa, Andre Miguel; Pereira, Carla; Sousa, Ana Berta;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
AUTHORS: Ramos Travessa, Andre Miguel; Pereira, Carla; Sousa, Ana Berta;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS
WOS29
TITLE: A NOVEL HOMOZYGOUS VARIANT IN CDK10-AL KAISSI SYNDROME AS AN EMERGING DISORDER Full Text
AUTHORS: Soares, Marta P.; Rodrigues, Marcia; Sousa, Ana Berta;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
AUTHORS: Soares, Marta P.; Rodrigues, Marcia; Sousa, Ana Berta;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS
WOS30
TITLE: TO REPORT OR NOT TO REPORT?-15Q11.2 (BP1-BP2) RECURRENT MICRODELETION Full Text
AUTHORS: Custodio, Sonia; Macedo, Catarina; Silveira Santos, Rosario; Rodrigues, Raquel; Rolo, Eva; Sousa, Ana Berta; Sousa, Ana;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
AUTHORS: Custodio, Sonia; Macedo, Catarina; Silveira Santos, Rosario; Rodrigues, Raquel; Rolo, Eva; Sousa, Ana Berta; Sousa, Ana;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS
WOS