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Artigo de periodico
ESICM guidelines on acute respiratory distress syndrome: definition, phenotyping and respiratory support strategies (2023)
Grasselli, Giacomo; Calfee, Carolyn S; Camporota, Luigi; Poole, Daniele; Amato, Marcelo Britto Passos ; Antonelli, Massimo; Arabi, Yaseen M; Baroncelli, Francesca; Beitler, Jeremy R; Bellani, Giacomo; Barbas, Carmen Silvia Valente
Fonte: Intensive care medicine. Unidade: FM
Assuntos: SÍNDROME DO DESCONFORTO RESPIRATÓRIO EM ADULTOS, GUIAS, PRÁTICA CLÍNICA, TERAPIA RESPIRATÓRIA
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ABNT
GRASSELLI, Giacomo et al. ESICM guidelines on acute respiratory distress syndrome: definition, phenotyping and respiratory support strategies. Intensive care medicine, v. 49, n. 7, p. 727-759, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/56020. Acesso em: 14 nov. 2024.
APA
Grasselli, G., Calfee, C. S., Camporota, L., Poole, D., Amato, M. B. P., Antonelli, M., et al. (2023). ESICM guidelines on acute respiratory distress syndrome: definition, phenotyping and respiratory support strategies. Intensive care medicine, 49( 7), 727-759. doi:10.1007/s00134-023-07050-7
NLM
Grasselli G, Calfee CS, Camporota L, Poole D, Amato MBP, Antonelli M, Arabi YM, Baroncelli F, Beitler JR, Bellani G, Barbas CSV. ESICM guidelines on acute respiratory distress syndrome: definition, phenotyping and respiratory support strategies [Internet]. Intensive care medicine. 2023 ; 49( 7): 727-759.[citado 2024 nov. 14 ] Available from: https://observatorio.fm.usp.br/handle/OPI/56020
Vancouver
Grasselli G, Calfee CS, Camporota L, Poole D, Amato MBP, Antonelli M, Arabi YM, Baroncelli F, Beitler JR, Bellani G, Barbas CSV. ESICM guidelines on acute respiratory distress syndrome: definition, phenotyping and respiratory support strategies [Internet]. Intensive care medicine. 2023 ; 49( 7): 727-759.[citado 2024 nov. 14 ] Available from: https://observatorio.fm.usp.br/handle/OPI/56020
Artigo de periodico
First theoretical framework for highly efficient photovoltaic parameters by structural modification with benzothiophene-incorporated acceptors in dithiophene based chromophores (2022)
Khalid, Muhammad; Ahmed, Rameez; shafq, Iqra; Arshad, Muhammad; Asghar, Muhammad Adnan; Munawar, Khurram Shahzad ; Imran, Muhammad; Braga, Ataualpa Albert Carmo
Fonte: Scientifc Reports. Unidades: FM, IQ
Assuntos: CÉLULAS SOLARES, DEPÓSITOS DE COMBUSTÍVEL FÓSSIL
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ABNT
KHALID, Muhammad et al. First theoretical framework for highly efficient photovoltaic parameters by structural modification with benzothiophene-incorporated acceptors in dithiophene based chromophores. Scientifc Reports, v. 12, p. 1-15 art. 20148 , 2022Tradução . . Disponível em: https://doi.org/10.1038/s41598-022-24087-8. Acesso em: 14 nov. 2024.
APA
Khalid, M., Ahmed, R., shafq, I., Arshad, M., Asghar, M. A., Munawar, K. S., et al. (2022). First theoretical framework for highly efficient photovoltaic parameters by structural modification with benzothiophene-incorporated acceptors in dithiophene based chromophores. Scientifc Reports, 12, 1-15 art. 20148 . doi:10.1038/s41598-022-24087-8
NLM
Khalid M, Ahmed R, shafq I, Arshad M, Asghar MA, Munawar KS, Imran M, Braga AAC. First theoretical framework for highly efficient photovoltaic parameters by structural modification with benzothiophene-incorporated acceptors in dithiophene based chromophores [Internet]. Scientifc Reports. 2022 ; 12 1-15 art. 20148 .[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/s41598-022-24087-8
Vancouver
Khalid M, Ahmed R, shafq I, Arshad M, Asghar MA, Munawar KS, Imran M, Braga AAC. First theoretical framework for highly efficient photovoltaic parameters by structural modification with benzothiophene-incorporated acceptors in dithiophene based chromophores [Internet]. Scientifc Reports. 2022 ; 12 1-15 art. 20148 .[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/s41598-022-24087-8
Artigo de periodico
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay (2021)
Melo, Uirá Souto ; Bonner, Devon ; Lloyd, Kevin C. Kent ; Moshiri, Ala ; Willis, Brandon ; Lanoue, Louise ; Bower, Lynette; Leonard, Brian C. ; Martins, Davi Jardim ; Gomes, Fernando ; Leite, Felipe de Souza ; Oliveira, Danyllo ; Kitajima, João Paulo; Monteiro, Fabiola P. ; Zatz, Mayana ; Menck, Carlos Frederico Martins ; Wheeler, Matthew T. ; Bernstein, Jonathan A. ; Dumas, Kevin; Spiteri, Elizabeth ; Di Donato, Nataliya ; Jahn, Arne ; Hashem, Mais; Alsaif, Hessa S. ; Chedrawi, Aziza; Alkuraya, Fowzan S. ; Kok, Fernando ; Byers, Heather M.
Fonte: Genetics in Medicine. Unidades: IB, ICB, FM
Assuntos: MICROBIOLOGIA, EXONS, GENOMAS, PESSOAS COM DEFICIÊNCIA INTELECTUAL, DOENÇAS DO DESENVOLVIMENTO ÓSSEO, VARIAÇÃO GENÉTICA
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ABNT
MELO, Uirá Souto et al. Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay. Genetics in Medicine, v. 23, n. 4, p. 6611-668, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41436-020-01047-z. Acesso em: 14 nov. 2024.
APA
Melo, U. S., Bonner, D., Lloyd, K. C. K., Moshiri, A., Willis, B., Lanoue, L., et al. (2021). Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay. Genetics in Medicine, 23( 4), 6611-668. doi:10.1038/s41436-020-01047-z
NLM
Melo US, Bonner D, Lloyd KCK, Moshiri A, Willis B, Lanoue L, Bower L, Leonard BC, Martins DJ, Gomes F, Leite F de S, Oliveira D, Kitajima JP, Monteiro FP, Zatz M, Menck CFM, Wheeler MT, Bernstein JA, Dumas K, Spiteri E, Di Donato N, Jahn A, Hashem M, Alsaif HS, Chedrawi A, Alkuraya FS, Kok F, Byers HM. Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay [Internet]. Genetics in Medicine. 2021 ; 23( 4): 6611-668.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/s41436-020-01047-z
Vancouver
Melo US, Bonner D, Lloyd KCK, Moshiri A, Willis B, Lanoue L, Bower L, Leonard BC, Martins DJ, Gomes F, Leite F de S, Oliveira D, Kitajima JP, Monteiro FP, Zatz M, Menck CFM, Wheeler MT, Bernstein JA, Dumas K, Spiteri E, Di Donato N, Jahn A, Hashem M, Alsaif HS, Chedrawi A, Alkuraya FS, Kok F, Byers HM. Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay [Internet]. Genetics in Medicine. 2021 ; 23( 4): 6611-668.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/s41436-020-01047-z
Artigo de periodico-carta/editorial
Definition, aims, and implementation of GA²2LEN/HAEi angioedema centers of reference and excellence. [Carta] (2020)
Maurer, Marcus; Aberer, Werner; Agondi, Rosana Camara ; Al‐Ahmad, Mona; Al‐Nesf, Maryam Ali; Ansotegui, Ignacio; Arnaout, Rand; Arruda, Luisa Karla de Paula ; Asero, Riccardo; Aygören‐Pürsün, Emel
Fonte: Allergy. Unidades: FM, FMRP
Assuntos: ANGIOEDEMA, URTICÁRIA, DERMATITE, INFORMAÇÃO EM SAÚDE, ALERGIA E IMUNOLOGIA
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ABNT
MAURER, Marcus et al. Definition, aims, and implementation of GA²2LEN/HAEi angioedema centers of reference and excellence. [Carta]. Allergy. West Sussex: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/all.14293. Acesso em: 14 nov. 2024. , 2020
APA
Maurer, M., Aberer, W., Agondi, R. C., Al‐Ahmad, M., Al‐Nesf, M. A., Ansotegui, I., et al. (2020). Definition, aims, and implementation of GA²2LEN/HAEi angioedema centers of reference and excellence. [Carta]. Allergy. West Sussex: Faculdade de Medicina, Universidade de São Paulo. doi:10.1111/all.14293
NLM
Maurer M, Aberer W, Agondi RC, Al‐Ahmad M, Al‐Nesf MA, Ansotegui I, Arnaout R, Arruda LK de P, Asero R, Aygören‐Pürsün E. Definition, aims, and implementation of GA²2LEN/HAEi angioedema centers of reference and excellence. [Carta] [Internet]. Allergy. 2020 ; 75( 8): 2115-2123.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1111/all.14293
Vancouver
Maurer M, Aberer W, Agondi RC, Al‐Ahmad M, Al‐Nesf MA, Ansotegui I, Arnaout R, Arruda LK de P, Asero R, Aygören‐Pürsün E. Definition, aims, and implementation of GA²2LEN/HAEi angioedema centers of reference and excellence. [Carta] [Internet]. Allergy. 2020 ; 75( 8): 2115-2123.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1111/all.14293
Artigo de periodico
Interobserver agreement of usual interstitial pneumonia diagnosis correlated with patient outcome (2016)
Hashisako, Mikiko; Tanaka, Tomonori; Terasaki, Yasuhiro; Uekusa, Toshimasa; Achcar, Rosane; Aswad, Bassam I.; Bamefleh, Hanna S.; Capelozzi, Vera Luiza; English, John C.; Fabro, Alexandre Todorovic
Fonte: Archives of Pathology and Laboratory Medicine. Unidades: FM, FMRP
Assuntos: FIBROSE PULMONAR, BIÓPSIA, PULMÃO, ANÁLISE DE SOBREVIVÊNCIA
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ABNT
HASHISAKO, Mikiko et al. Interobserver agreement of usual interstitial pneumonia diagnosis correlated with patient outcome. Archives of Pathology and Laboratory Medicine, v. 140, n. 12, p. 1375-1382, 2016Tradução . . Disponível em: https://doi.org/10.5858/arpa.2016-0012-OA. Acesso em: 14 nov. 2024.
APA
Hashisako, M., Tanaka, T., Terasaki, Y., Uekusa, T., Achcar, R., Aswad, B. I., et al. (2016). Interobserver agreement of usual interstitial pneumonia diagnosis correlated with patient outcome. Archives of Pathology and Laboratory Medicine, 140( 12), 1375-1382. doi:10.5858/arpa.2016-0012-OA
NLM
Hashisako M, Tanaka T, Terasaki Y, Uekusa T, Achcar R, Aswad BI, Bamefleh HS, Capelozzi VL, English JC, Fabro AT. Interobserver agreement of usual interstitial pneumonia diagnosis correlated with patient outcome [Internet]. Archives of Pathology and Laboratory Medicine. 2016 ; 140( 12): 1375-1382.[citado 2024 nov. 14 ] Available from: https://doi.org/10.5858/arpa.2016-0012-OA
Vancouver
Hashisako M, Tanaka T, Terasaki Y, Uekusa T, Achcar R, Aswad BI, Bamefleh HS, Capelozzi VL, English JC, Fabro AT. Interobserver agreement of usual interstitial pneumonia diagnosis correlated with patient outcome [Internet]. Archives of Pathology and Laboratory Medicine. 2016 ; 140( 12): 1375-1382.[citado 2024 nov. 14 ] Available from: https://doi.org/10.5858/arpa.2016-0012-OA
Artigo de periodico
Identification and Treatment of Patients with Homozygous Familial Hypercholesterolaemia: Information and Recommendations from a Middle East Advisory Panel (2015)
Al-Ashwal, Abdullah; Alnouri, Fahad; Sabbour, Hani; Al-Mahfouz, Abdulraof; Al-Sayed, Nasreen; Razzaghy-Azar, Maryam; Al-Allaf, Faisal; Al-Waili, Khalid; Banerjee, Yajnavalka; Genest, Jacques; Santos, Raul D.; Al-Rasadi, Khalid
Fonte: Current Vascular Pharmacology. Unidade: FM
Assuntos: DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA, HIPERCOLESTEROLEMIA
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ABNT
AL-ASHWAL, Abdullah et al. Identification and Treatment of Patients with Homozygous Familial Hypercholesterolaemia: Information and Recommendations from a Middle East Advisory Panel. Current Vascular Pharmacology, v. 13, n. 6, p. 759-770, 2015Tradução . . Disponível em: https://doi.org/10.2174/1570161113666150827125040. Acesso em: 14 nov. 2024.
APA
Al-Ashwal, A., Alnouri, F., Sabbour, H., Al-Mahfouz, A., Al-Sayed, N., Razzaghy-Azar, M., et al. (2015). Identification and Treatment of Patients with Homozygous Familial Hypercholesterolaemia: Information and Recommendations from a Middle East Advisory Panel. Current Vascular Pharmacology, 13( 6), 759-770. doi:10.2174/1570161113666150827125040
NLM
Al-Ashwal A, Alnouri F, Sabbour H, Al-Mahfouz A, Al-Sayed N, Razzaghy-Azar M, Al-Allaf F, Al-Waili K, Banerjee Y, Genest J, Santos RD, Al-Rasadi K. Identification and Treatment of Patients with Homozygous Familial Hypercholesterolaemia: Information and Recommendations from a Middle East Advisory Panel [Internet]. Current Vascular Pharmacology. 2015 ; 13( 6): 759-770.[citado 2024 nov. 14 ] Available from: https://doi.org/10.2174/1570161113666150827125040
Vancouver
Al-Ashwal A, Alnouri F, Sabbour H, Al-Mahfouz A, Al-Sayed N, Razzaghy-Azar M, Al-Allaf F, Al-Waili K, Banerjee Y, Genest J, Santos RD, Al-Rasadi K. Identification and Treatment of Patients with Homozygous Familial Hypercholesterolaemia: Information and Recommendations from a Middle East Advisory Panel [Internet]. Current Vascular Pharmacology. 2015 ; 13( 6): 759-770.[citado 2024 nov. 14 ] Available from: https://doi.org/10.2174/1570161113666150827125040

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