×
Close
Sign Up
Login
Home
Library S
Library D
Events & Partner
WeMed
MDLA Events Platform
Events
Media Partners
Educational Partner
User Tools
FAQ/USER GUIDE
Language
English
中文/ Chinese
French
Português
Español
Arabic
Russian
Contact Us
×
Close
mdla_1
mdla_2
mdla_3
mdla_4
mdla_5
mdla_6
Categories
Genetics & Heredity
15176
Global Medical University
5161
Allergy
1838
Anatomy & Morphology
1606
Andrology
414
Anesthesia & Intensive Care
1274
Anesthesiology
5632
Audiology & Speech-Language Pathology
369
Behavioral Sciences
100
Biochemical Research Methods
7099
Biochemistry & Molecular Biology
30128
Biodiversity Conservation
321
Biology
8489
Biophysics
8298
Biotechnology & Applied Microbiology
8523
Cardiac & Cardiovascular Systems
31423
Cardiovascular & Respiratory Systems
1418
Cell & Tissue Engineering
693
Cell Biology
11185
Chemistry, Analytical
4315
Chemistry, Applied
11079
Chemistry, Medicinal
8707
Chemistry, Multidisciplinary
18684
Clinical Immunology & Infectious Disease
468
Clinical Medicine
8936
Clinical Neurology
16774
Clinical Psychology & Psychiatry
1327
Critical Care Medicine
3235
Dentistry, Oral Surgery & Medicine
13491
Dermatology
7641
Developmental Biology
7022
Ecology
662
Education, Scientific Disciplines
2010
Emergency Medicine
4123
Endocrinology, Metabolism & Nutrition
24521
Engineering, Biomedical
3749
Entomology
438
Environmental Medicine & Public Health
4732
Evolutionary Biology
271
Gastroenterology & Hepatology
12390
General & Internal Medicine
7077
Geriatrics & Gerontology
5263
Gerontology
360
Health Care Sciences & Services
16168
Health Policy & Services
637
Hematology
5659
Immunology
25042
Infectious Diseases
14027
Integrative & Complementary Medicine
2913
Medical Ethics
1206
Medical Informatics
2259
Medical Laboratory Technology
433
Medicine, General & Internal
44907
Medicine, Legal
533
Medicine, Research & Experimental
17852
Microbiology
23313
Mycology
0
Nanoscience & Nanotechnology
5329
Neuroimaging
1395
Neurology
4572
Neurosciences
40128
Nursing
9741
Nutrition & Dietetics
7945
Obstetrics & Gynecology
8338
Oncology
52767
Ophthalmology
9796
Optics
4250
Orthopedics
11804
Orthopedics, Rehabilitation & Sports Medicine
1805
Otolaryngology
1558
Otorhinolaryngology
4931
Parasitology
1105
Pathology
5142
Pediatrics
21747
Peripheral Vascular Disease
4924
Pharmacology & Pharmacy
35300
Pharmacology/Toxicology
12199
Physiology
9036
Polymer Science
559
Primary Health Care
872
Psychiatry
19282
Psychology
5281
Psychology, Applied
111
Psychology, Biological
355
Psychology, Clinical
805
Psychology, Developmental
236
Psychology, Educational
159
Psychology, Experimental
158
Psychology, Mathematical
0
Psychology, Multidisciplinary
1688
Psychology, Psychoanalysis
41
Psychology, Social
121
Public Health & Health Care Science
2286
Public, Environmental & Occupational Health
27501
Quantum Science & Technology
0
Radiology, Nuclear Medicine & Imaging
12505
Radiology, Nuclear Medicine & Medical Imaging
8104
Rehabilitation
3097
Remote Sensing
0
Reproductive Biology
2859
Reproductive Medicine
1181
Research/Laboratory Medicine & Medical Technology
3987
Respiratory System
7499
Rheumatology
6043
Social Sciences, Biomedical
1227
Substance Abuse
2752
Surgery
34206
Toxicology
4377
Transplantation
955
Tropical Medicine
314
Urology & Nephrology
13183
Veterinary Sciences
35
Virology
2457
Zoology
0
Channels
INTERNATIONAL JOURNAL OF NEONATAL SCREENING
89
Genetics
5
NEJM Genetics
3
Medrxiv - Genetic And Genomic Medicine
1770
CANCER GENE THERAPY
368
CHROMOSOMA
74
CLINICAL GENETICS
118
CURRENT GENETICS
122
CURRENT OPINION IN GENETICS & DEVELOPMENT
265
EPIGENETICS & CHROMATIN
136
EPIGENOMICS
33
EPILEPSIA
211
FRONTIERS IN GENETICS
5440
GENE THERAPY
184
GENETICS IN MEDICINE
104
GENOME MEDICINE
308
GENOMICS PROTEOMICS & BIOINFORMATICS
215
HUMAN GENETICS
349
HUMAN MUTATION
121
JOURNAL OF HUMAN GENETICS
291
JOURNAL OF MEDICAL GENETICS
411
NATURE REVIEWS GENETICS
326
NPJ GENOMIC MEDICINE
185
ORPHANET JOURNAL OF RARE DISEASES
795
ANNALS OF HUMAN GENETICS
24
CYTOGENETIC AND GENOME RESEARCH
97
G3-GENES GENOMES GENETICS
19
GENETIC EPIDEMIOLOGY
30
HUMAN GENOMICS
232
HUMAN HEREDITY
33
INTERNATIONAL JOURNAL OF IMMUNOGENETICS
23
JOURNAL OF EVOLUTIONARY BIOLOGY
120
JOURNAL OF GENETIC COUNSELING
152
PSYCHIATRIC GENETICS
131
EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS
278
FORENSIC SCIENCE INTERNATIONAL GENETICS SUPPLEMENT SERIES
17
GENETICS AND MOLECULAR RESEARCH
22
GLOBAL MEDICAL GENETICS
158
JOURNAL OF COMMUNITY GENETICS
200
NON-CODING RNA
125
FUNCTIONAL & INTEGRATIVE GENOMICS
513
GENETICA
112
IMMUNOGENETICS
143
JOURNAL OF APPLIED GENETICS
222
JOURNAL OF GENETICS
193
RUSSIAN JOURNAL OF GENETICS
409
SCI Abstract
search
ALL
RECOMMENDED
+
IJNS, Vol. 9, Pages 2: Newborn Screening Long-Term Follow-Up Clinics (Continuity Clinics) in the Philippines during the COVID-19 Pandemic: Continuing Quality Patient Care
The COVID-19 pandemic has challenged healthcare systems worldwide. In the Philippines, long-term care for patients with co...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 9, Pages 1: Remembering the Legacy of Judi Tuerck
Judith “Judi” Tuerck, RN, MS, one of the true pioneers in the development of newborn screening (NBS), ...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 66: A Retrospective Evaluation of the Predictive Value of Newborn Screening for Vitamin B12 Deficiency in Symptomatic Infants Below 1 Year of Age
Background: The sensitivity of newborn screening (NBS) in detecting infants that later develop symptomatic vitamin B12 def...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 64: Technical Study of Automated High-Throughput High-Sensitive Ceruloplasmin Assay on Dried Blood Spots—Reinstate the Potential Use for Newborn Screening of Wilson Disease
In this study, we modified a fully automatic immunoassay on ceruloplasmin concentration on dried blood spots (DBS) to incr...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 63: Assessing the Content Quality of Online Parental Resources about Newborn Metabolic Disease Screening: A Content Analysis
Parents increasingly utilise the internet to obtain information on health practices, but the quality of online information...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 60: Inconsistent Provider Testing Practices for Congenital Cytomegalovirus: Missed Diagnoses and Missed Opportunities
Newborn congenital cytomegalovirus (cCMV) screening programs have been found to increase the rates of early diagnosis and ...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 61: A Roadmap for Potential Improvement of Newborn Screening for Inherited Metabolic Diseases Following Recent Developments and Successful Applications of Bivariate Normal Limits for Pre-Symptomatic Detection of MPS I, Pompe Disease, and Krabbe Disease
The mucopolysaccharidoses (MPS), Pompe Disease (PD), and Krabbe disease (KD) are inherited conditions known as lysosomal s...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 59: Parental Depression and Anxiety Associated with Newborn Bloodspot Screening for Rare and Variable-Onset Disorders
The ability to screen newborns for a larger number of disorders, including many with variable phenotypes, is prompting deb...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 57: Multiple 17-OHP Cutoff Co-Variates Fail to Improve 21-Hydroxylase Deficiency Screening Accuracy
To improve the positive predictive value (PPV) of newborn screening for 21-hydroxylase deficiency (21OHD), co-variates hav...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 58: Missed Cystic Fibrosis Newborn Screening Cases due to Immunoreactive Trypsinogen Levels below Program Cutoffs: A National Survey of Risk Factors
Testing immunoreactive trypsinogen (IRT) is the first step in cystic fibrosis (CF) newborn screening. While high IRT is as...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 56: Evaluation of a New Laboratory Protocol for Newborn Screening for Congenital Adrenal Hyperplasia in New Zealand
Between 2005 and 2021, 49 cases of classical congenital adrenal hyperplasia were diagnosed in New Zealand, 39 were detecte...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 50: Newborn Screening for Duchenne Muscular Dystrophy: First Year Results of a Population-Based Pilot
Advancements in therapies for Duchenne muscular dystrophy (DMD) have made diagnosis within the newborn period a high prior...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 54: Parental Preferences about Policy Options Regarding Disclosure of Incidental Genetic Findings in Newborn Screening: Using Videos and the Internet to Educate and Obtain Input
Our objective was to develop and test a new approach to obtaining parental policy guidance about disclosure of incidental ...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 53: Psychosocial Issues Related to Newborn Screening: A Systematic Review and Synthesis
Genomic advances have contributed to a proliferation of newborn screening (NBS) programs. Psychosocial consequences of NBS...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 49: Developing an Online Dashboard to Visualize Performance Data—Tennessee Newborn Screening Experience
Newborn screening (NBS) is a vital public health program and delays in the screening process can lead to catastrophic outc...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 48: dbRUSP: An Interactive Database to Investigate Inborn Metabolic Differences for Improved Genetic Disease Screening
The Recommended Uniform Screening Panel (RUSP) contains more than forty metabolic disorders recommended for inclusion in u...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 47: Expanded Newborn Screening in Italy Using Tandem Mass Spectrometry: Two Years of National Experience
Newborn screening (NBS) for inborn errors of metabolism is one of the most advanced tools for secondary prevention in medi...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 46: Impact of Pancreatitis-Associated Protein on Newborn Screening Outcomes and Detection of CFTR-Related Metabolic Syndrome (CRMS)/Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID): A Monocentric Prospective Pilot Experience
Pancreatitis-Associated Protein (PAP)-based Cystic Fibrosis (CF) newborn bloodspot screening (NBS) protocols detect less C...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 45: Modelling the Cost-Effectiveness and Budget Impact of a Newborn Screening Program for Spinal Muscular Atrophy and Severe Combined Immunodeficiency
Spinal muscular atrophy (SMA) and severe combined immunodeficiency (SCID) are rare, inherited genetic disorders with sever...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 44: Economic Evaluation of Newborn Screening for Severe Combined Immunodeficiency
Evidence on the cost-effectiveness of newborn screening (NBS) for severe combined immunodeficiency (SCID) in the Australia...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 39: Experience of the NPC Brazil Network with a Comprehensive Program for the Screening and Diagnosis of Niemann-Pick Disease Type C
Niemann-Pick disease type C (NPC) is a lysosomal disorder caused by impaired cholesterol metabolism. Levels of lysosphingo...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 37: William Harry Hannon—A Life Well Lived
Dr [...]
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 33: Introducing Newborn Screening for Severe Combined Immunodeficiency—The New Zealand Experience
Screening for severe combined immunodeficiency (SCID) was added to the New Zealand national newborn screening programme in...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 34: Use of Online Newborn Screening Educational Resources for the Education of Expectant Parents: An Improvement in Equity
Educating parents about the newborn screening (NBS) process is critical in ensuring that families are aware of their child...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 32: A Public Dialogue to Inform the Use of Wider Genomic Testing When Used as Part of Newborn Screening to Identify Cystic Fibrosis
Cystic fibrosis (CF) has been included within the UK national newborn screening programme since 2007. The approach uses me...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 27: Newborn Screen for X-Linked Adrenoleukodystrophy Using Flow Injection Tandem Mass Spectrometry in Negative Ion Mode
X-linked adrenoleukodystrophy (X-ALD) is a genetic disorder caused by pathogenic variants in the ATP-binding cassette subf...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 25: A New Approach to Objectively Evaluate Inherited Metabolic Diseases for Inclusion on Newborn Screening Programmes
Newborn screening (NBS) programmes are essential in the diagnosis of inherited metabolic diseases (IMDs) and for access to...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 24: Newborn Screening for X-Linked Adrenoleukodystrophy: Review of Data and Outcomes in Pennsylvania
X-linked adrenoleukodystrophy (X-ALD) is the most common peroxisomal disorder. It results from pathogenic variants in ABCD...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 23: Improving Recruitment for a Newborn Screening Pilot Study with Adaptations in Response to the COVID-19 Pandemic
Seven months after the launch of a pilot study to screen newborns for Duchenne Muscular Dystrophy (DMD) in New York State,...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
IJNS, Vol. 8, Pages 22: Ethical Considerations for Equitable Access to Genomic Sequencing for Critically Ill Neonates in the United States
Rare diseases impact all socio-economic, geographic, and racial groups indiscriminately. Newborn screening (NBS) is an exe...
International Journal Of Neonatal Screening
comment
0
thumb_up
0
Load More
Modal title
×
Modal title
×
Share
Login
Global News and Health Forum
Join Now!
Member Login
Remember me
Forgot password?
Or using
Linkedin