Cargando…

Thalassemias: can we reduce the national burden?

Detalles Bibliográficos
Autor principal:	Colah, Roshan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2014
Materias:	Speaker Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042365/ https://www.ncbi.nlm.nih.gov/pubmed/24940367 http://dx.doi.org/10.1186/1755-8166-7-S1-I43

Ejemplares similares

Community genetics approaches in the prevention of beta-thalassemia: towards achieving ‘Zero beta-thalassemia’ status in India
por: Rao, V R
Publicado: (2014)

Should we avoid protease inhibitors in first lines due to their lipid side effects? - cons
por: Stellbrink, Hans-Jürgen
Publicado: (2014)

Addressing health and ageing in the German national health monitoring system
por: Scheidt-Nave, Christa, et al.
Publicado: (2013)

Current status of sickle cell disease in India: how can you attenuate?
por: Mohanty, Dipika
Publicado: (2014)

Headache research - where are we heading?
por: Jensen, Rigmor
Publicado: (2013)

Disability, ICF biopsychosocial model and burden of migraine
por: Leonardi, Matilde, et al.
Publicado: (2015)

Early exposure hypothesis: where are we now?
por: Lack, Gideon
Publicado: (2011)

Do we need to demonstrate Amyloid in tissue?
por: Magy, Laurent
Publicado: (2015)

Genomics-based breeding in forest trees: are we there yet?
por: Neale, David
Publicado: (2011)

Genome-forward oncology: how do we get there?
por: Ellis, Matthew
Publicado: (2011)

Is RBC discrimination index suitable for differentiating between α- and β- thalassemias?
por: Gorakshakar, Ajit C., et al.
Publicado: (2011)

Do we need to demonstrate amyloid in tissue for hereditary ATTR amyloidosis ?
por: Westermark, Per
Publicado: (2015)

The national registration and accreditation scheme
por: Warnock, Jason, et al.
Publicado: (2011)

Recruitment to trials - why is it hard and how might we make it less so?
por: Treweek, Shaun
Publicado: (2011)

PReS13-SPK-1582: Activity and damage - we have to measure them
por: Feldman, BM
Publicado: (2013)

PReS13-SPK-1028: Activity and damage - we have to measure them
por: Brunner, H
Publicado: (2013)

Significance of borderline HbA(2) levels in β thalassemia carrier screening
por: Colaco, Stacy, et al.
Publicado: (2022)

Hydrocephalus treatment and outcome in African infants with myelomeningocele: what we have learned so far
por: Warf, Benjamin C
Publicado: (2010)

Cascade screening for β-thalassemia: A practical approach for identifying and counseling carriers in India
por: Gorakshakar, Ajit C, et al.
Publicado: (2009)

I-2 Can we bypass a muscle metabolic defect?
por: Argov, Z.
Publicado: (2011)

PReS13-SPK-1247: Activity and damage in juvenile systemic sclerosis- we have to measure them
por: Foeldvari, I
Publicado: (2013)

A proposal for a national registry on chronic migraines
por: Vanacore, Nicola, et al.
Publicado: (2015)

Prenatal screening for Mendelian disorders in antenatal care
por: Verma, Amar
Publicado: (2014)

Functional genomics of lung cancer progression reveals mechanism of metastasis suppressor function
por: Thakur, Ram Krishna, et al.
Publicado: (2014)

Newborn screening- the roadmap for India
por: Kapoor, Seema
Publicado: (2014)

Non-coding RNA based regulation of blood vessel development in zebrafish and relevance to humans
por: Sivasubbu, Sridhar
Publicado: (2014)

Digital health, microfluidics, and bedside genetic testing
por: Hashsham, Syed
Publicado: (2014)

Genomic packaging and epigenetic regulation of genes
por: Mishra, Rakesh
Publicado: (2014)

Mitochondrial donation by stem cells: potential for novel therapeutics
por: Agrawal, Anurag
Publicado: (2014)

Detection and Inheritance Pattern of Copy Number Variations (CNVs) in Children with Multiple Congenital Anomalies
por: Sheth, Frenny
Publicado: (2014)

Dysmorphology of inborn errors of metabolism
por: Kimonis, Virginia
Publicado: (2014)

Genomic copy number variations in glaucomatous neurodegeneration
por: Mukhopadhyay, Arijit
Publicado: (2014)

G protein signaling in tumor cell growth and metastasis
por: Dhanasekaran, Danny
Publicado: (2014)

Human variome project – current overview
por: Cotton, Richard
Publicado: (2014)

In search of epi-driver genes in head and neck cancer
por: Bhattacharjya, Sumana, et al.
Publicado: (2014)

Exome sequencing in unspecific intellectual disability and rare disorders
por: Rauch, Anita
Publicado: (2014)

Consanguinity and perinatal medicine - the berlin perspective
por: Becker, Rolf
Publicado: (2014)

Uniparental disomy - clinical consequences due to imprinting and activation of recessive genes
por: Liehr, Thomas
Publicado: (2014)

Prakruti genomics and prameha-proclivity: relevance to metabolic syndrome
por: Vaidya, Ashok DB
Publicado: (2014)

Microdeletion syndromes
por: Datar, Chaitanya
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_om8ujmpc1hp0071btft8s7hgc6