21
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
INDEXED IN: WOS
22
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
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID
23
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
INDEXED IN: Scopus WOS CrossRef: 5
IN MY: ORCID
24
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
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID
25
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
INDEXED IN: WOS
26
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
INDEXED IN: WOS
27
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
INDEXED IN: WOS
28
TITLE: GENOTYPE, PHENOTYPE AND CLINICAL FOLLOW-UP OF A MULTICENTRIC COHORT OF PATIENTS WITH PTEN HAMARTOMA TUMOR SYNDROME  Full Text
AUTHORS: Soares, Celia Azevedo; Soares, Gabriela; Soares, Ana Rita; Soares, Marta; Rodrigues, Marcia; Dupont, Juliette; Dias, Patricia; Soeiro e Sa, Mariana; Sousa, Ana Berta; Nunes, Sofia; Venancio, Margarida; Antunes, Diana; Fortuna, Ana Maria; Tkachenko, Natalia;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS
29
TITLE: TAB2 HAPLOINSUFFICIENCY - FROM ISOLATED HEART DISEASE TO A NEWLY RECOGNIZED SYSTEMIC PATTERN  Full Text
AUTHORS: Silva, Raquel Gouveia; Moldovan, Oana; Rebelo, Monica; Sérgio Matoso Laranjo; Sousa, Ana Berta;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS
30
TITLE: THREE PATIENTS WITH PHIP-RELATED SYNDROME - FURTHER PHENOTYPIC DELINEATION  Full Text
AUTHORS: Macedo, Catarina; Soeiro e Sa, Mariana; Dias, Patricia; Rodrigues, Marcia; Sousa, Ana Berta;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS
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