Results 101 to 110 of about 292,301 (384)

Midwifery basics. Infant feeding: Managing baby related challenges [PDF]

, 2013
Infant feeding: is the twelfth series of ‘Midwifery basics’ targeted at practising midwives. It aims to provide information to raise awareness of the impact of the work of midwives on women’s experience and encourage midwives to seek further information ...
Marshall, Joyce
core  

A companion to the preclinical common data elements for proteomics, lipidomics, and metabolomics data in rodent epilepsy models. A report of the TASK3‐WG4 omics working group of the ILAE/AES joint translational TASK force

Epilepsia Open, EarlyView., 2022
Abstract The International League Against Epilepsy/American Epilepsy Society (ILAE/AES) Joint Translational Task Force established the TASK3 working groups to create common data elements (CDEs) for various preclinical epilepsy research disciplines.
Laura Bindila, Tore Eid, James D. Mills, Michael S. Hildebrand, Gary P. Brennan, Susan A. Masino, Vicky Whittemore, Piero Perucca, Christopher A. Reid, Manisha Patel, Kevin K. Wang, Erwin A. van Vliet   +11 more
wiley   +1 more source

Diagnostic and predictive ability of hyperbilirubinemia severity in cats: A multicenter retrospective study

Journal of Veterinary Internal Medicine
Background Total serum bilirubin concentration (TBIL) can provide useful information on several pathophysiological conditions in cats. Nevertheless, whether the variable severity classification of hyperbilirubinemia can reliably indicate certain disease ...
Xavier Salord Torres, Kamalan Jeevaratnam, Imogen Schofield, Samantha Taylor, Jennifer Stallwood, Menai Heyes, Daniel Hughes, Pieter Defauw   +7 more
doaj   +1 more source

Nursing protocol for neonatal phototherapy [PDF]

, 2017
Objetivo: Determinar la evidencia disponible en el manejo de fototerapia para el tratamiento de ictericia neonatal para construir un protocolo de enfermería.
Castaño Picó, María José, Sánchez Maciá, Miriam   +1 more
core   +1 more source

The Behavioral Phenotype and Importance of Multidisciplinary Care in Patients With Sotos Syndrome: A Single‐Center Experience

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Sotos syndrome is an autosomal dominant condition caused by pathogenic variants in the NSD1 gene on chromosome 5q35. It is characterized by macrosomia, distinctive facial features, and developmental delays. Patients are also reported to have a behavioral phenotype including autism spectrum disorder, attention deficit/hyperactivity disorder ...
Aravind Viswanathan, Andrew M. George, Evan R. Hathaway, Carlyn Glatts, Jennifer M. Kalish   +4 more
wiley   +1 more source

Signal Quality in Continuous Transcutaneous Bilirubinometry

Sensors
Bilirubin is a product of the metabolism of hemoglobin from red blood cells. Higher levels of bilirubin are a sign that either there is an unusual breaking down rate of red blood cells or the liver is not able to eliminate bilirubin, through bile, into ...
Fernando Crivellaro, Anselmo Costa, Pedro Vieira   +2 more
doaj   +1 more source

Comparative study of the clinical manifestations and pathophysiology of leptospirosis and scrub typhus [PDF]

, 2009
The study aims were to determine the prevalence of leptospirosis and scrub typhus in northeast Thailand, and to compare and contrast their clinical features and outcomes.
Chierakul, Wirongrong
core   +1 more source

Piscine reovirus, but not Jaundice Syndrome, was transmissible to Chinook Salmon, Oncorhynchus tshawytscha (Walbaum), Sockeye Salmon, Oncorhynchus nerka (Walbaum), and Atlantic Salmon, Salmo salar L.

Journal of Fish Diseases, 2016
A Jaundice Syndrome occurs sporadically among sea-pen-farmed Chinook Salmon in British Columbia, the westernmost province of Canada. Affected salmon are easily identified by a distinctive yellow discolouration of the abdominal and periorbital regions ...
K. Garver, G. Marty, S. Cockburn, J. Richard, L. Hawley, A. Müller, R. L. Thompson, M. Purcell, S. Saksida   +8 more
semanticscholar   +1 more source

AP2M1 Is a Candidate Gene for Microcephaly and Intellectual Disability in 3q27.1 Deletions

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Deletions of the 3q26.33q27.2 region appear to correlate with a distinct phenotype, although there are few reported cases. Here, we present seven previously unreported individuals carrying de novo 3q27 deletions (under 5 Mb), which include the AP2M1 (adaptor‐related protein complex 2, mu‐1 subunit) gene and summarize data from 12 previously ...
Russell Gear, Paul Kalitsis, Melissa Glass, Bertrand Isidor, Catherine Vincent‐Delorme, Florence Petit, Judith M. A. Verhagen, Alexander Jorge, Ana Cristina Victorino Krepischi, Ikeoluwa Osei‐Owusu, Eva Martinez, Anne O'Donnell‐Luria, Nicole de Leeuw, Sarah Ruggiero, Ingo Helbig, Francis David I, Natasha J. Brown   +16 more
wiley   +1 more source

A young patient with Graves' disease presenting with a triad of heart failure, pancytopenia, and jaundice: A case report

Clinical Case Reports
Key Clinical Message Graves's disease must be treated promptly to avoid serious sequelae such as cardiomyopathy, liver injury, and pancytopenia. Early initiation of antithyroid medications and beta blockers could not be overrated even in the presence of ...
Mohamed Kamal Sabra, Anwar Joudeh, Mahmoud Al Niserat, Riyadh Hammamy   +3 more
doaj   +1 more source