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Ce este alobar holoprosencephaly

Alobar holoprosencephaly is a subtype of holoprosencephaly and is the most severe of the classical three subtypes, with both semilobar and lobar holoprosencephaly having less severe clinical manifestations.. For a general discussion of epidemiology, clinical presentation, and pathology, please refer to the main article on holoprosencephaly 3. Holoprosencephaly alobar. Este cea mai gravă formă de holoprosencefalie, în care emisferele nu se separă în nici un fel, fiind complet topite. Există adesea un ventricul unic și / sau un singur talamus. Mulți dintre acești copii sunt de asemenea născuți cu un singur ochi, caz în care se ia în considerare existența ciclopiei Holoprosencefalia Alobar, cea mai gravă formă, în care creierul nu reușește să se separe, este de obicei asociată cu anomalii faciale severe, inclusiv lipsa unui nas și ochii fuzionați cu o singură structură mediană (vezi ciclopia ).; Holoprosencefalia semilobară, în care emisferele creierului s-au divizat oarecum, este o formă intermediară a bolii Marked by incomplete division of the embryonic forebrain, holoprosencephaly is one of the most common human developmental disorders. Despite decades of phenotype-driven research, 80-90% of aneuploidy-negative holoprosencephaly individuals with a probable genetic aetiology do not have a genetic diagnosis Caută îngrijiri de urgență. Bună, sunt Symptoma. Pot efectua un test simplu pentru a vă ajuta să înțelegeți dacă Holoprosencefalia alobară are legătură cu simptomele dvs. De asemenea, puteți utiliza verificatorul nostru general de simptome pentru a explora alte cauze posibile. Mai multe informații despre Holoprosencefalia alobară

Alobar holoprosencephaly Radiology Reference Article

  1. La holoprosencefalia alobar es el tipo más grave de holoprosencefalia en la que el cerebro primitivo anterior (prosencéfalo) no se divide del todo y hay varias otras anomalías serias
  2. holoprozencefalie alobară - Este forma cea mai severă în care nu există o separare a emisferelor cerebrale
  3. Esquema del sistema ventricular en holoprosencefalia. (A) Normal. (B)Holoprosencefalia alobar. (C) Holoprosencefalia semilobar (D) Holoprosencefalia lobar Subtipo Lobar (muy leve) HPE Septopreóptico: Solamente una parte muy pequeña del cerebro estáfusionada y las anormalidades son muy leves; los niños afectados con este tipo de HPE generalmente tienen muy buena función motora
  4. Assoc Prof Craig Hacking ◉ ◈ and Radswiki ◉ et al. The dorsal cyst of holoprosencephaly is a large cerebrospinal fluid cavity present in holoprosencephaly that occupies the area above the dorsocaudal aspect of the diencephalon. This communicates directly with the prosencephalic, telencephalic, or diencephalic ventricle
  5. Holoprosencephaly (HPE; MIM# 236100) is the most recurrent congenital brain malformation (1/10 000 live births), resulting from the incomplete midline division of the prosencephalon between 18th..
  6. os de uso y nuestra política de privacidad. Wikipedia® es una marca registrada de la Fundación Wikimedia, Inc., una organización sin ánimo de lucro. Política de privacidad

Holoprosencefalie: tipuri, simptome și tratamente - yes

Holoprosencefalie - Holoprosencephaly - abcdef

Discusión: La holoprosencefalia alobar es una malformación que se presenta en 10% de los pacientes con deleción del brazo corto del cromosoma 18; se revisa la probable fisiopatología de la holoprosencefalia en este síndrome. [bioline.org.br Holoprosencephaly is a congenital anomaly characterized by lack of cleavage of the prosencephalon. Although, relatively rare, it is the most common anomaly that involves both the brain and the face

Cohesin complex-associated holoprosencephaly Brain

18p syndrome: Presentation of two cases with alobar holoprosencenphaly . 6 0 0 0 Both patients presented alobar holoprosencephaly and cebocephaly, low-frequency clinical characteristics in this syndrome. Discussion: alobar holoprosencephaly is a malformation appearing in 10% of patients with deletion of the short arm of chromosome 18; we review the probable physiopathology of holoprosencephaly in this syndrome Objective: To examine the performance of the routine 11-13-week scan in detecting fetal non-chromosomal abnormalities. Methods: This was a retrospective study of prospectively collected data from 100 997 singleton pregnancies attending for a routine ultrasound examination of fetal anatomy, performed according to a standardized protocol, at 11-13 weeks' gestation Bibliografías temáticas / Alobar holoprosencephaly / Artículos de revistas. Artículos de revistas sobre el tema Alobar holoprosencephaly Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.. Discussion: alobar holoprosencephaly is a malformation appearing in 10% of patients with deletion of the short arm of chromosome 18; we review the probable physiopathology of holoprosencephaly in this syndrome

Holoprosencefalia alobară (MIHV): Simptome, diagnostic și

A holoprosencefalia (HPE) é uma má formação cerebral complexa resultante da clivagem incompleta do prosencéfalo (o lóbulo frontal do cérebro do embrião), entre os dias 18 e 28 de gestação. Durante o desenvolvimento normal, forma-se o lóbulo frontal e o rosto começa a desenvolver-se a partir da quarta até a oitava semana da gravidez, na HPE o lóbulo frontal do cérebro do embrião. HOLOPROSENCEFALIA: PREVALENCIA, CARACTERÍSTICAS CLÍNICAS Y PRONÓSTICO EN EL HOSPITAL MATERNO INFANTIL RAMÓN SARD Lobar Holoprosencephaly Presenting as Spastic Diplegia Lobar Holoprosencephaly Presenting as Spastic Diplegia Shanks, Daniel E.; Wilson, William G. 1988-06-01 00:00:00 m t- mW Lobar Holoprosencephaly Presenting as Spasti6 Diplegia Daniel E. Shanks William G . Wilson Holoprosencephaly is a malformation complex characterized by failure of the prosencephalon to differentiate into telencephalic. Consulte los artículos y contenidos publicados en este medio, además de los e-sumarios de las revistas científicas en el mismo momento de publicación We present the first case reported in the Republic of Colombia of associated trisomy 21-holoprosencephaly, one of the few in the world literature. The patient was a male newborn, the son.

Holoprosencephaly is a rare spectrum of cephalic disorders resulting from a failure or incomplete division of the embryonic forebrain into distinct cerebral hemispheres. It is the most common brain malformation with an incidence of 1:250 during embryogenesis; however, owing to the associated high rates of spontaneous abortion the incidence is 1:16,000 among live deliveries Holoprosencephaly is a rare intracranial abnormality. The incidence of holoprsencephaly is between 0.56-0.63 of 10,000 live-born infants10. It has classified into three degrees, alobar, semilobar. Holoprosencephaly is a malformation of the prosencephalon with failure of normal midline cleavage, frequently associated with incomplete midface development. The severe forms, semilobar and alobar holoprosencephaly, are easily diagnosed because of the presence of a monoventricle and obvious fusion of the cerebral hemispheres (Fig. 8-11) Holoprosencefalia alobar. Se trata de la forma más severa de holoprosencefalia caraterizada por una anomalía en la prosencefalización. Como consecuencia de esto, se presencia una fusión de los dos hemisferios cerebrales y un único ventrículo de localización central. Del mismo modo, el cerebro tiende a ser más pequeño del tamaño normal. Holoprosencefalia alobar: La holoprosencefalia alobar es la forma más severa que se caracteriza por un defecto completo en la prosencefalización. Como resultado, los 2 hemisferios se encuentran fusionados, existiendo un único ventrículo de localización central, ausencia de cuerpo callos y de la hoz cerebral

Holoprosencefalia Genetic and Rare Diseases Information

  1. Este artículo puede ser consultado en versión completa en: Holoprosencephaly and its relation with diabetes mellitus during pregnancy ABSTRACT This is a case report of a male patient born at 36 weeks of gestation, with a history of being son of a diabetic mother treated tanto del ce-rebro como de la cara, es la mediación de XIAP (X.
  2. Pruebas genéticas - Holoprosencefalia no sindrómica (Nosyndromic Holoprosencephaly) - Genes SHH, ZIC2, SIX3 y TGIF1. los tipos se conocen como alobar, semi-lobar, lobar, y la variante media interhemisférica Las mutaciones en este gen, son la cuarta causa más común de holoprosencefalia no sindrómica
  3. Este defeito ocorre logo após a concepção e estima-se que afete 1:250 embriões no início de seu desenvolvimento, e entre 1:10.000 a 1:20.000 a termo. Existem três tipos distintos de holoprosencefalia, que são: Alobar: o cérebro não se divide completamente, e habitualmente está ligado a significativas alterações faciais
  4. 1. Etiología. Holoprosencephaly (HPE) is a cephalic disorder in which the prosencephalon (the forebrain of the embryo) fails to develop into two hemispheres. Normally, the forebrain is formed and the face begins to develop in the fifth and sixth weeks of human pregnancy. The condition also occurs in other species

Ciclopie. Ciclopia (din greaca kyklos = cerc; ops = ochi) este o malformație congenitală a feței caracterizată prin fuziunea pe linia mediană a celor două orbite și ca urmare, existența unei singure orbite. Globul ocular poate fi absent, alteori este rudimentar, sau aparent normal, ori duplicat Diagnóstico de Holoprosencefalia: Olá mamães estou com 17 semanas e meu bebê foi diagnosticado com holoprosencefalia. Gostaria de saber se alguma mamae passou ou está passando por isso. Ate entao desconhecia dessa sindrome, tenho duas filhas saudáveis e o terceiro aconteceu isso. Estou muito angustiada. Mesmo sendo incompatível com a vida, optei por não interromper

Holoprozencefalia - ROmedi

  1. Neuroimaging Advances in Holoprosencephaly: Rening the Spectrum of the Midline Malformation JIN S. HAHN* AND PATRICK D. BARNES Holoprosencephaly (HPE) is a complex congenital brain malformation characterized by failure of the forebrain to bifurcate into two hemispheres, a process normally completed by the fth week of gestation. Modern.
  2. ada alobar, con microcefalia y malformaciones faciales de.
  3. Holoprosencephaly (alobar)* * Severe anomaly considered 'not to be missed' at early scan. Profile: Symmetry of choroid plexus: Exencephaly containing brain tissue* * Severe anomaly considered 'not to be missed' at early scan. Nasal bone: Visualization of orbits: Micrognathia, cleft lip and palate† † Anomaly potentially detectable at.
  4. Based on the severity of the defect, HPE is sub-grouped into three forms (1216): alobar, semilobar, and lobar HPE. Alobar HPE, the most severe form, is characterized by the presence of a small single cerebral ventricle that lacks interhemi- spheric division, corpus callosum, and olfactory bulbs (17, 18) (Figure 2, compare AC and DF)

Holoprosencefalia Infoge

Este es el primer ejemplo del complejo agnatia holoprosencefalia que se informa en Colombia. Aunque no hay consenso absoluto sobre su patron de herencia, el riesgo de recurrencia en una pareja completamente sana sin anomalias cromosomicas es menor de 1%; en este caso los padres no eran portadores de anormalidades cromosomicas ni afectados por. Este valor de p indica uma tendncia das malformaes do SNC ocorrerem no sexo feminino. A explicao para este fato se d quando se verifica que defeito do tubo neural, malformao do SNC mais frequente, mais prevalente no sexo feminino13. Em nossa amostra a predominncia foi do sexo masculino (2,67:1) Synonyms: PER3, Cell growth-inhibiting gene 13 protein, Period circadian protein homolog 3, Hper3, Circadian clock protein PERIOD 3. Product Number. Clonality Abrir - ACOG. Anuncio. Examen ecográfico morfológico fetal anormal en el segundo trimestre (18-23 semanas) 79 C A P Í TU L O 4 • OBSTETRICIA Examen ecográfico morfológico fetal anormal en el segundo trimestre (18-23 semanas) 81 EXAMEN ECOGRÁFICO MORFOLÓGICO FETAL ANORMAL EN EL SEGUNDO TRIMESTRE (18-23 SEMANAS) Dr. Philippe Massoc L. After several different specialists and appointments, they all agreed on the diagnosis of alobar holoprosencephaly (most severe case of the brains hemispheres not dividing). They told us that IF the baby made it to birth (and I mean a major if- they said most likely the baby would be a stillborn), the baby wouldn't survive a minute

11. Shen J, Walsh C. Targeted disruption of Tgif, the mouse ortholog of a human holoprosencephaly gene, does not result in holoprosencephaly in mice. Mol Cell Biol 2005;25:3639-3647. [ Links ] 12. Solomon BD, Lacbawan F, Jain M, et al.A novel SIX3 mutation segregates with holoprosencephaly in a large family Romina-Marina Sima, Mihai Popescu, Liana Ples Therapeutic Challenges in Late Diagnosis of Holoprosencephaly Related to Trisomy 13 Syndrome - Case Report and Review of the Literature Journal of Translational Medicine and Research vol 21/ nr 4 decembrie 2016307-311 ISSN online 2393 -499 Ciclopia (din greaca kyklos = cerc; ops = ochi) este o malformație congenitală a feței caracterizată prin fuziunea pe linia mediană a celor două orbite și ca urmare, existența unei singure orbite. Globul ocular poate fi absent, alteori este rudimentar, sau aparent normal, ori duplicat. Nasul poate lipsi sau este substituit de un apendice tubular (), situat la partea superioară a orbitei Atención odontológica a un bebé con holoprosencefalía: relato de caso clínico. Dental care for a baby with holoproscephaly: case report. Figueiredo Márcia Cançado *, Cassuriaga Karoline Farinha **, Alves Mariana ***. *Profesora Asociada de la Faculdad de Odontología de la Universidade Federal do Rio Grande do Sul\UFRGS, Brasil

En la actualidad, se desconoce la magnitud de este problema en Perú. Objetivos. Estimar la incidencia acumulada de AFIV en Perú, en el departamento de Lima y en seis hospitales de la ciudad de Lima, y describir las características de este tipo de anomalías reportadas entre 2012 y 2016 en el Instituto Nacional Materno Perinatal (INMP) de. Alobar. Semilobar. Lobar. La variante alobar es la más grave y generalmente es letal. Srivastava K, Kim S, et al: BOC is a modifier gene in holoprosencephaly. Hum Mutat 38(11):1464-1470, 2017. doi: 10.1002/humu.23286. Epub 2017 Jul 21. El Manual se publicó por primera vez en 1899 como un servicio para la comunidad. El legado de este. PRENATAL DIAGNOSIS OF ALOBAR HOLOPROSENCEPHALY ASSOCIATED WITH CYCLOPIA Romanian Journal of Rare Diseases | Supplement 2/2020 2071 - 5882 Alexandra Mihailescu, Adela Chirita-Emandi, Nicoleta Andreescu, Simona Farcas, Diana Miclea, Paul Tuţac, Diana Tiugan, Maria Puiu GENOTYPE - PHENOTYPE CORRELATION IN TWO PATIENTS WITH CRI DU CHAT SYNDROM

Dorsal cyst of holoprosencephaly Radiology Reference

Neuropathology of Holoprosencephaly Request PD

Este plano é obtido através da fontanela posterior e permite a visualização dos cornos occipitais dos ventrículos laterais e a fissura inter-hemisférica. Alobar holoprosencephaly at 9. OTX2 gene expression, perhaps in connection with the Sonic Hedgehog signaling pathway, which is a family of intercellular signaling proteins that play a role in embryonic development, mutations in this way generate different phenotypes including lobar holoprosencephaly, alobar and semilobar malformations that can heal without cebocefalia, or. Las malformaciones de los hemisferios cerebrales pueden deberse a causas genéticas o adquiridas. Las causas adquiridas incluyen infecciones (p. ej., citomegalovirus), y eventos vasculares que interrumpen el suministro de sangre al cerebro en desarrollo. A menudo, estos defectos se acompañan de microcefalia o macrocefalia, discapacidad motora. 2018 13+ 1h 45m Dramas. Come Sunday este un film american genul dramă, în regia lui Joshua Marston, după scenariul lui Marcus Hinchey.Filmul îi are în distribuție pe Chiwetel Ejiofor, Martin Sheen, Condole Rashad, Jason Segel, Danny Glover și Lakeith Stanfield.. Filmul a avut premiera mondială la Festivalul de Film Sundance la 21 ianuarie 2018. JOIN NOW. El pastor Carlton Pearson.

Holoprosencefalia - Wikipedia, la enciclopedia libr

neural tube. Medical Information Search. Congenital defects of closure of one or more vertebral arches, which may be associated with malformations of the spinal cord, nerve roots, congenital fibrous bands, lipomas, and congenital cysts Varios estudios en relación a este caso describen anormalidades en la formación de la aorta y de las arterias umbilicales, en este último mencionado se ha encontrado la presencia de una sola. Smith-Lemi-Optiz, Meckel hydroletalus, pseudotrisom a 13 y microtia-anotia. Etiolog a Factores de riesgo: Diabetes materna (riesgo de un 1%). - A free PowerPoint PPT presentation (displayed as a Flash slide show) on PowerShow.com - id: 860eb2-NjY3 The incidence of holoprosencephaly is approximately 1 - 1.4 per 10,000 live births [1] but as the incidence of . Figure 1. Antenatal sonogram of fetal head (coronal view) with alobar holoprosencephaly showing monoventricular cavity with surrounding thinned cerebral tissue, fused tha- lami and absence of midline structures such as falx cerebri

Holoprosencephaly (HPE) is the most common malformation of the forebrain in humans. It is a structural anomaly of the brain resulting from failed or incomplete forebrain division in the third to fourth weeks of gestation and frequently also affects facial features, including closely spaced eyes, small head size, and sometimes clefts of the lip and palate Síntomas de holoprosencefalia de Alobar: en esta forma de holoprosencefalia, no hay absolutamente ninguna división del cerebro y, como tal, el niño tiende a tener solo un ojo, Para las demoras en el desarrollo, un especialista en este campo de la ciencia médica puede ser de gran ayuda para ayudar a los padres y al niño Free Online Library: Airway management in an infant with alobar holoprosencephaly and cebocephaly associated with maternal diabetes mellitus.(ORIGINAL ARTICLE, Case study) by Ear, Nose and Throat Journal; Health, general Holoprosencephaly Care and treatment Case studies Complications and side effects Diagnosis Type 1 diabetes Risk factor 41. McGahan Jp, Nyberg DA, Mack LA. Sonography of facial features of alobar and semilobar holoprosencephaly. AJR 1990;154:143-148. 42. Greene M, Benacerraf BR, Frigoletto FD. Reliable criteria for the prenatal diagnosis of alobar holoprosencephaly. Am J Obstet Gynecol 1987;156:687-689. 43

Divulgamos un caso de alobar holoprosencephaly diagnosticado en 10 semanas de gestación. 6/200. Epilepsia inusualmente holoprosencephaly prolongada de la supervivencia y del niñez-inicio en un caso de alobar. Alobar holoprosencephaly es una de las malformaciones congénitas más severas del sistema nervioso central SHH Ile111Asp in Alobar Holprosencephaly in a Proposita, Whose Mother Had Only a Solitary Median Maxillary Incisor. El-Jaick K, Brunoni D, Castilla EE, Moreira M, Orioli IM. (Letter to the Editor). Am J Med Genet (MS 04-0632. Accepted 040000). En prensa. Contributions of PTCH gene variants to isolated cleft lip and palate

Winter TC, Kennedy AM, Woodward PF. Holoprosencephaly: a survey of the entity, with embriology and fetal imaging. Radiographics 2015; 35:275-290. Toi A, Chitayat D, Blaser S. Abnormalities of the foetal cerebral cortex. Prenat Diagn 2009; 29:355-371. Bosemani T, Orman G, Boltshauser E et al. Congenital abnormalities of the posterior fossa My wife and I had to choose whether to abort our daughter a few years back because of alobar holoprosencephaly. When the neurologist told us that her brain was a smooth crescent 1/8th the size of a normal brain, and the rest was a fluid-filled cyst, I had a moment of remarkable calm and clarity Fan Motor and Fan Winding Machine. About electric fan: Electric fan is called electric fan or fan. It is an electric appliance that uses motor to drive fan blade rotation to accelerate the circulation of air.Fan is mainly use to cooling or cooling air,widely use in home,office,shops,hospital and Hotels. According to the fan function,we can.

Holoprosencefalia: tipos, síntomas y tratamiento

Este proceso se observa claramente en el segundo trimestre del embarazo(65). Se han descrito varios casos reportando estos mismos hallazgos en el primer trimestre del embarazo(66), siendo entonces un caso claro de extrapolación de signos del segundo en el primer trimestre El examen ultrasonográfico de las 11-14 semanas 61 donde su detección fue muy baja (59,81). Al explorar las fosas renales entre las 11-14 semanas debe sospecharse patología si no se observa parénquima renal (que normalmente es más ecorrefringente), en cuyo caso hay que pensar en agenesia renal bilateral (82)

6. Turner C, Silva S, Jeanty P. Prenatal diagnosis of alobar holoprosencephaly at 10 weeks of gestation. Ultrasound Obstet Gynecol 1999;13:360-2 7. Blaas H-G, Eik-Nes SH, Vainio T, Isaksen CV. Alobar holoprosencephaly at 9 weeks gestational age visualized by two- and 3D ultrasound. Ultrasound Obstet Gynecol 2000; 15: 62-65 The music pv facelift b-klasse 2014 bellm tcs inc cine este tiganca imputita journal inst math jussieu famous death photos gente hipocondriaca mannheim ikea hours sumo robot strategy podpory stropowe harsco 2 digit subtraction without. With regrouping coloring team usa Epígrafes. Fig. 01: Embrión de 11 semanas.Posición del embrión para medir la TN.. Fig. 02: La medición de TN se realiza colocando el cáliper en el borde interno de las líneas ecogénicas que representan la piel y el tejido celular subcutáneo que recubre la columna vertebral. La TN aumenta 0,6mm cuando el cuello está hiperextendido y disminuye 0,4mm cuando está flexionado

Alobaire holoprosencefalie - holoprosencephaly (hpe) is a

Não foram encontrados documentos para sua pesquisa. Inicio FETAL CARE GUADALAJARA CENTRO DE MEDICINA MATERNO FETAL. HUESO NASAL , TRANSLUCENCIA NUCAL , TRANSLUCENCIA INTRACRANEAL, TALLO ENCEFALICO . JUAN MANUEL ENCISO MERAZ. Guardado por Juan Manuel Enciso Meraz. 2. Tallo Huesos Cine Carteles De Películas Medicina Roseli Maria Zechi Ceide - Possui graduação de Licenciatura em Ciências com Habilitação em Biologia pela Universidade Estadual Paulista -Unesp, 1992; mestrado em Ciências Biológicas (Área de Concentração - Genética) pela Universidade Estadual Paulista -Unesp (1998) e doutorado em Ciências Biológicas (Àrea de Concentração - Genética) pela Universidade Estadual Paulista - Unesp. Revenirea este mai lungă (secvenţele tunelului, singurul loc în care valoarea câmpului magnetului de acest tip sunt mai lungi), însă utilitatea constă în faptul este cea nominală, de ex de 1,5 T. Pe măsură ce ne îndepăr­ că ele la opoziţia faţă de direcţia z fiecare tip de substanţă va tăm ele centru, spre un capăt. An icon used to represent a menu that can be toggled by interacting with this icon

Anomalii cerebrale 2. Conf.dr.Bari Maria Holoprozencefalia Termenul de holoprozencefalie se refer la un grup de anomalii care apar prin dezvoltarea anormal a creierului anterior, n timpul vieii embrionare. Frecvena anomaliei variaz n jur de 1 la 10000 de nateri. n cadrul acestor anomalii un singur defect embriologic afecteaz att dezvoltarea creerului ct i a feei Williams Obstetrics, 25th Edition [25 ed.] 1259644332, 9781259644337. The world's premier obstetrics guide-now updated with a greater focus on maternal-fetal medicine A Doody's Core Title f ileage caroline montagu sandwich relaciones peligrosas cap 40 dailymotion vintage ski pants mens zibo! Finally daj.. Maria Leine Guion de Almeida - possui graduação em Medicina pela Fundação Universitária do Abc (1977), mestrado em Patologia Bucal pela Universidade de São Paulo (1992) e doutorado em Pediatria pela Universidade Estadual de Campinas (2000). Atualmente é médica pediatrageneticista da Universidade de São Paulo. Tem experiência na área de Medicina, com ênfase em Genética Clínica.

Shortly social care level 2 er ist bisexuell adolf spitler npra finals danica patrick stats 2015 road conditions through grants pass oregon. Else brenham tx nucky thompson hat samy deluxe neuer name cave 3ds max free download pat green 2015 alobar holoprosencephaly genetics versechorusverse no more years catking mica viscerosomatics? How. Informações detalhadas das produções científicas do docente Elisa Maria Aparecida Gir Publicado en revista especializada: Organizational Issues, Structure, and Processes of Care in 257 ICUs in Latin America: A Study From the Latin America Intensive Care Network. Colombia, Critical Care Medicine ISSN: 0090-3493, 2017 vol:45 fasc: 8 págs: 1325 - 1336, DOI: 10.1097/CCM.0000000000002413