Results 111 to 120 of about 1,400 (148)
Guidelines on the Diagnosis and Treatment of Hypertrophic Cardiomyopathy - 2024. [PDF]
Arq Bras CardiolFernandes F, Simões MV, Correia EB, Marcondes-Braga FG, Coelho-Filho OR, Mesquita CT, Mathias Junior W, Antunes MO, Arteaga-Fernández E, Rochitte CE, Ramires FJA, Alves SMM, Montera MW, Lopes RD, Oliveira Junior MT, Scolari FL, Avila WS, Canesin MF, Bocchi EA, Bacal F, Moura LZ, Saad EB, Scanavacca MI, Valdigem BP, Cano MN, Abizaid AAC, Ribeiro HB, Lemos Neto PA, Ribeiro GCA, Jatene FB, Dias RR, Beck-da-Silva L, Rohde LEP, Bittencourt MI, Pereira ADC, Krieger JE, Villacorta Junior H, Martins WA, Figueiredo Neto JA, Cardoso JN, Pastore CA, Jatene IB, Tanaka ACS, Hotta VT, Romano MMD, Albuquerque DC, Mourilhe-Rocha R, Hajjar LA, Brito Junior FS, Caramelli B, Calderaro D, Farsky PS, Colafranceschi AS, Pinto IMF, Vieira MLC, Danzmann LC, Barberato SH, Mady C, Martinelli Filho M, Torbey AFM, Schwartzmann PV, Macedo AVS, Ferreira SMA, Schmidt A, Melo MDT, Lima Filho MO, Sposito AC, Brito FS, Biolo A, Madrini Junior V, Rizk SI, Mesquita ET. +71 moreeuropepmc +1 more sourceA unique case of hereditary bilateral segmental neurofibromatosis on the face [PDF]
Agarwal A, Crowe FW, Dimitrije Jankovic, Dogra S, Gammel JA, Hager CM, Irena Jankovic, Maldonado Cid P, Milan Visnjic, Milena Velickovic, Miller RM, Oguzkan S, Predrag Kovacevic, Riccardi VM, Stolarczuk DA +14 morecore +1 more sourceFeocromocitona: presentación de un caso y revisión parcial de la literatura [PDF]
, 1974 Alberola, V., Labios, M., Losada, J. A., Marín, J., O'Connor, C., Pascual-Leone, A., Valdés Ruiz, M. +6 morecore Brazilian Guidelines for In-office and Out-of-office Blood Pressure Measurement - 2023. [PDF]
Arq Bras CardiolFeitosa ADM, Barroso WKS, Mion Junior D, Nobre F, Mota-Gomes MA, Jardim PCBV, Amodeo C, Oliveira AC, Alessi A, Sousa ALL, Brandão AA, Pio-Abreu A, Sposito AC, Pierin AMG, Paiva AMG, Spinelli ACS, Machado CA, Poli-de-Figueiredo CE, Rodrigues CIS, Forjaz CLM, Sampaio DPS, Barbosa ECD, Freitas EV, Cestario EDES, Muxfeldt ES, Lima Júnior E, Campana EMG, Feitosa FGAM, Consolim-Colombo FM, Almeida FA, Silva GVD, Moreno Júnior H, Finimundi HC, Guimarães ICB, Gemelli JR, Barreto-Filho JAS, Vilela-Martin JF, Ribeiro JM, Yugar-Toledo JC, Magalhães LBNC, Drager LF, Bortolotto LA, Alves MAM, Malachias MVB, Neves MFT, Santos MC, Dinamarco N, Moreira Filho O, Passarelli Júnior O, Vitorino PVO, Miranda RD, Bezerra R, Pedrosa RP, Paula RB, Okawa RTP, Póvoa RMDS, Fuchs SC, Lima SG, Inuzuka S, Ferreira-Filho SR, Fillho SHP, Jardim TSV, Guimarães Neto VDS, Koch VHK, Gusmão WDP, Oigman W, Nadruz Junior W. +66 moreeuropepmc +1 more sourceSome of the next articles are maybe not open access.Related searches:
La neurofibromatose de type I : à propos de dix observations
Annales d'Endocrinologie, 2014 Introduction La NFI est frequente. Elle est genetique autosomique dominante responsable de troubles de la differenciation du tissu ectodermique. Si le diagnostic est facile chez l’adulte, sa reconnaissance est tardive chez l’enfant Nous rapportons a ce propos 10 observations. Observations Six enfants d’age moyen 9,5 ans (7–11), deux adolescents de A.E.M. Haddam, N.S. Fedala, H. Si Youcef, F. Chentli, D. Meskine, N. Fedala +5 moreopenaire +1 more source
