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TITLE: Social Support and Cognitive Impairment: Results from a Portuguese 4-Year Prospective Study  Full Text
AUTHORS: Pais, R; Ruano, L ; Moreira, C ; Fraga, S ; Carvalho, OP; Barros, H ;
PUBLISHED: 2021, SOURCE: INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, VOLUME: 18, ISSUE: 16
INDEXED IN: Scopus WOS CrossRef: 5
IN MY: ORCID
2
TITLE: Global cognitive impairment prevalence and incidence in community dwelling older adults—a systematic review
AUTHORS: Pais, R; Ruano, L ; Carvalho, OP; Barros, H;
PUBLISHED: 2020, SOURCE: Geriatrics (Switzerland), VOLUME: 5, ISSUE: 4
INDEXED IN: Scopus CrossRef Handle
IN MY: ORCID
3
TITLE: Prevalence and incidence of cognitive impairment in an elder Portuguese population (65-85 years old)
AUTHORS: Pais, R; Ruano, L ; Moreira, C ; Carvalho, OP; Barros, H ;
PUBLISHED: 2020, SOURCE: BMC GERIATRICS, VOLUME: 20, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID
4
TITLE: Bone formation and resorption markers at 7 years of age: Relations with growth and bone mineralization
AUTHORS: Monjardino, T; Silva, P; Amaro, J ; Carvalho, O; Guimaraes, JT ; Santos, AC ; Lucas, R ;
PUBLISHED: 2019, SOURCE: PLOS ONE, VOLUME: 14, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID
5
TITLE: A novel disorder reveals clathrin heavy chain-22 is essential for human pain and touch development
AUTHORS: Michael S Nahorski; Lihadh Al-Gazali; Jozef Hertecant; David J Owen; Georg H H Borner; Ya-Chun Chen; Caroline L Benn; Ofélia P Carvalho; Samiha S Shaikh; Anne Phelan; Margaret S Robinson; Stephen J Royle; Geoffrey G Woods;
PUBLISHED: 2015, SOURCE: Brain, VOLUME: 138, ISSUE: 8
INDEXED IN: CrossRef: 43
IN MY: ORCID
6
TITLE: Transcriptional regulator PRDM12 is essential for human pain perception
AUTHORS: Ya-Chun Chen; Michaela Auer-Grumbach; Shinya Matsukawa; Manuela Zitzelsberger; Andreas C Themistocleous; Tim M Strom; Chrysanthi Samara; Adrian W Moore; Lily Ting-Yin Cho; Gareth T Young; Caecilia Weiss; Maria Schabhüttl; Rolf Stucka; Annina B Schmid; Yesim Parman; Luitgard Graul-Neumann; Wolfram Heinritz; Eberhard Passarge; Rosemarie M Watson; Jens Michael Hertz; Ute Moog; Manuela Baumgartner; Enza Maria Valente; Diego Pereira; Carlos M Restrepo; Istvan Katona; Marina Dusl; Claudia Stendel; Thomas Wieland; Fay Stafford; Frank Reimann; Katja von Au; Christian Finke; Patrick J Willems; Michael S Nahorski; Samiha S Shaikh; Ofélia P Carvalho; Adeline K Nicholas; Gulshan Karbani; Maeve A McAleer; Maria Roberta Cilio; John C McHugh; Sinead M Murphy; Alan D Irvine; Uffe Birk Jensen; Reinhard Windhager; Joachim Weis; Carsten Bergmann; Bernd Rautenstrauss; Jonathan Baets; Peter De Jonghe; Mary M Reilly; Regina Kropatsch; Ingo Kurth; Roman Chrast; Tatsuo Michiue; David L H Bennett; Geoffrey G Woods; Jan Senderek; ...More
PUBLISHED: 2015, SOURCE: Nature Genetics, VOLUME: 47, ISSUE: 7
INDEXED IN: CrossRef: 134
IN MY: ORCID
7
TITLE: A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy
AUTHORS: Carvalho, OP; Thornton, GK; Hertecant, J; Houlden, H; Nicholas, AK; Cox, JJ; Rielly, M; Al Gazali, L; Woods, CG;
PUBLISHED: 2011, SOURCE: Journal of Medical Genetics, VOLUME: 48, ISSUE: 2
INDEXED IN: Scopus CrossRef
IN MY: ORCID
8
TITLE: The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis
AUTHORS: Bakircioglu, M; Carvalho, OP; Khurshid, M; Cox, JJ; Tuysuz, B; Barak, T; Yilmaz, S; Caglayan, O; Dincer, A; Nicholas, AK; Quarrell, O; Springell, K; Karbani, G; Malik, S; Gannon, C; Sheridan, E; Crosier, M; Lisgo, SN; Lindsay, S; Bilguvar, K; Gergely, F; Gunel, M; Woods, CG; ...More
PUBLISHED: 2011, SOURCE: American Journal of Human Genetics, VOLUME: 88, ISSUE: 5
INDEXED IN: Scopus CrossRef
IN MY: ORCID
9
TITLE: A primary microcephaly protein complex forms a ring around parental centrioles  Full Text
AUTHORS: Sir, JH; Barr, AR; Nicholas, AK; Carvalho, OP; Khurshid, M; Sossick, A; Reichelt, S; D'Santos, C; Woods, CG; Gergely, F;
PUBLISHED: 2011, SOURCE: Nature Genetics, VOLUME: 43, ISSUE: 11
INDEXED IN: Scopus CrossRef: 103
IN MY: ORCID
10
TITLE: WDR62 is associated with the spindle pole and is mutated in human microcephaly  Full Text
AUTHORS: Nicholas, AK; Khurshid, M; Desir, J; Carvalho, OP; Cox, JJ; Thornton, G; Kausar, R; Ansar, M; Ahmad, W; Verloes, A; Passemard, S; Misson, JP; Lindsay, S; Gergely, F; Dobyns, WB; Roberts, E; Abramowicz, M; Woods, CG;
PUBLISHED: 2010, SOURCE: Nature Genetics, VOLUME: 42, ISSUE: 11
INDEXED IN: Scopus CrossRef
IN MY: ORCID
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