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1. Full Text Epicutaneous immunotherapy for the treatment of peanut allergy in children and young adults
by Jones, Stacie M., MD and Sicherer, Scott H., MD and Burks, A. Wesley, MD and Leung, Donald Y.M., MD and Lindblad, Robert W., MD and Dawson, Peter, PhD and Henning, Alice K., MS and Berin, M. Cecilia, PhD and Chiang, David, MSc and Vickery, Brian P., MD and Pesek, Robbie D., MD and Cho, Christine B., MD and Davidson, Wendy F., PhD and Plaut, Marshall, MD and Sampson, Hugh A., MD and Wood, Robert A., MD and Consortium Food Allergy Res and Consortium of Food Allergy Research
Journal of allergy and clinical immunology, ISSN 0091-6749, 2016, Volume 139, Issue 4, pp. 1242 - 1252.e9
Allergy and Immunology | epicutaneous | Peanut hypersensitivity | food allergy | IgE | desensitization | immunotherapy | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Transdermal Patch | Double-Blind Method | Humans | Child, Preschool | Male | Peanut Hypersensitivity - therapy | Young Adult | Allergens - administration & dosage | Adolescent | Adult | Female | Child | Desensitization, Immunologic - methods | Evaluation | Medical colleges | Stock options | Communicable diseases | Analysis | Immunotherapy | Peanut allergy | Drug therapy | Immunoglobulin E | Food allergies | Antigens | Young adults | Dendritic cells | Cytokines | Peanuts | Immunoglobulin G | Hypersensitivity | Clinical trials | Lymphocytes T | FDA approval | Asthma | Proteins | Side effects | Protein folding | Adults | Children | Age | Food | Index Medicus | Abridged Index Medicus
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2. Full Text Newborn screening for X-linked adrenoleukodystrophy: evidence summary and advisory committee recommendation
by Kemper, Alex R and Brosco, Jeffrey and Comeau, Anne Marie and Green, Nancy S and Grosse, Scott D and Jones, Elizabeth and Kwon, Jennifer M and Lam, Wendy K.K and Ojodu, Jelili and Prosser, Lisa A and Tanksley, Susan
Genetics in medicine, ISSN 1098-3600, 01/2017, Volume 19, Issue 1, pp. 121 - 126
dried blood spot testing public health | evidence-based practice | neonatal screening | adrenoleukodystrophy | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | New York | United States | Humans | United States Dept. of Health and Human Services | ATP Binding Cassette Transporter, Sub-Family D, Member 1 - genetics | Adrenoleukodystrophy - pathology | Male | Neonatal Screening | Advisory Committees | Phenotype | Adrenoleukodystrophy - diagnosis | Female | Adrenoleukodystrophy - genetics | Mutation | Infant, Newborn | Index Medicus
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3. Full Text Congenital cytomegalovirus infection in pregnancy and the neonate: consensus recommendations for prevention, diagnosis, and therapy
by Rawlinson, William D, Prof and Boppana, Suresh B, Prof and Fowler, Karen B, Prof and Kimberlin, David W, Prof and Lazzarotto, Tiziana, Prof and Alain, Sophie, Prof and Daly, Kate and Doutré, Sara and Gibson, Laura, Prof and Giles, Michelle L, PhD and Greenlee, Janelle and Hamilton, Stuart T, PhD and Harrison, Gail J, Prof and Hui, Lisa, PhD and Jones, Cheryl A, Prof and Palasanthiran, Pamela, Prof and Schleiss, Mark R, Prof and Shand, Antonia W, MD and van Zuylen, Wendy J, PhD
The Lancet infectious diseases, ISSN 1473-3099, 2017, Volume 17, Issue 6, pp. e177 - e188
Infectious Disease | Life Sciences & Biomedicine | Infectious Diseases | Science & Technology | Cytomegalovirus - isolation & purification | Hearing Loss, Sensorineural - congenital | Hearing Loss, Sensorineural - virology | Congenital Abnormalities - prevention & control | Hearing Loss, Sensorineural - prevention & control | Humans | Developmental Disabilities - prevention & control | Cytomegalovirus Infections - diagnosis | Congenital Abnormalities - virology | Mothers | Consensus | Congenital Abnormalities - diagnosis | Pregnancy | Cytomegalovirus Infections - prevention & control | Hearing Loss, Sensorineural - diagnosis | Pregnancy Complications, Infectious - prevention & control | Cytomegalovirus Infections - therapy | Female | Cytomegalovirus Infections - transmission | Cytomegalovirus Infections - congenital | Infectious Disease Transmission, Vertical - prevention & control | Infant, Newborn | Pregnancy Complications, Infectious - diagnosis | Prevention | Infants (Newborn) | Cytomegalovirus infections | Genetic disorders | Pregnant women | Health aspects | Neonates | Identification methods | Prophylaxis | Nervous system | Infections | Vaccines | Guidelines | Literature reviews | Newborn babies | Diagnosis | Public health | Cytomegalovirus | Congenital diseases | Group dynamics | Hearing impairment | Medical screening | Hearing loss | Disease prevention | Studies | Screening | Infectious diseases | Researchers | Womens health | Diagnostic systems | Health risk assessment | Index Medicus
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4. Full Text High baseline levels of tumor necrosis factor receptor 1 are associated with progression of kidney disease in indigenous australians with diabetes: The eGFR follow-up study
by Barr, Elizabeth L.M and Barzi, Federica and Hughes, Jaquelyne T and Jerums, George and Hoy, Wendy E and O'Dea, Kerin and Jones, Graham R.D and Lawton, Paul D and Brown, Alex D.H and Thomas, Mark and Ekinci, Elif I and Sinha, Ashim and Cass, Alan and MacIsaac, Richard J and Maple-Brown, Louise J
Diabetes care, ISSN 0149-5992, 04/2018, Volume 41, Issue 4, pp. 739 - 747
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Complications and side effects | Usage | Tumor necrosis factor inhibitors | Development and progression | Kidney diseases | Diabetes | Diagnosis | Risk factors | Urine | Creatinine | Tumor necrosis factor receptors | C-reactive protein | Kidneys | Epidermal growth factor receptors | Diabetes mellitus | Health risks | Hazards | Hip | Glomerular filtration rate | Proteins | Tumor necrosis factor | Tumor necrosis factor receptor 1 | Tumor necrosis factor-TNF | Blood pressure | Research design | Tumors | Index Medicus
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5. Full Text Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes
by Dorschner, Michael O and Amendola, Laura M and Turner, Emily H and Robertson, Peggy D and Shirts, Brian H and Gallego, Carlos J and Bennett, Robin L and Jones, Kelly L and Tokita, Mari J and Bennett, James T and Kim, Jerry H and Rosenthal, Elisabeth A and Kim, Daniel S and Tabor, Holly K and Bamshad, Michael J and Motulsky, Arno G and Scott, C. Ronald and Pritchard, Colin C and Walsh, Tom and Burke, Wylie and Raskind, Wendy H and Byers, Peter and Hisama, Fuki M and Nickerson, Deborah A and Jarvik, Gail P and National Heart, Lung, and Blood Institute Grand Opportunity Exome Sequencing Project and Natl Heart Lung And Blood Inst and Grand Opportunity Exome Sequencing
American journal of human genetics, ISSN 0002-9297, 10/2013, Volume 93, Issue 4, pp. 631 - 640
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Exome | Genetic Predisposition to Disease | Disease - genetics | Gene Frequency | Humans | Databases, Genetic | Incidental Findings | Penetrance | Polymorphism, Single Nucleotide | Research | Nucleotide sequencing | Gene expression | Genomics | DNA sequencing | Genomes | Biological variation | Mutation | Index Medicus
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6. Full Text De Novo Mutations in MLL Cause Wiedemann-Steiner Syndrome
by Jones, Wendy D and Dafou, Dimitra and McEntagart, Meriel and Woollard, Wesley J and Elmslie, Frances V and Holder-Espinasse, Muriel and Irving, Melita and Saggar, Anand K and Smithson, Sarah and Trembath, Richard C and Deshpande, Charu and Simpson, Michael A
American journal of human genetics, ISSN 0002-9297, 08/2012, Volume 91, Issue 2, pp. 358 - 364
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Medical genetics | Abnormalities, Multiple - pathology | Haploinsufficiency - genetics | Hypertrichosis - congenital | Growth Disorders - pathology | Histone-Lysine N-Methyltransferase | Humans | Molecular Sequence Data | Mutation - genetics | Sequence Analysis, DNA | Exome - genetics | Hypertrichosis - genetics | Myeloid-Lymphoid Leukemia Protein - genetics | Base Sequence | Hypertrichosis - pathology | Gene Components | Growth Disorders - genetics | Abnormalities, Multiple - genetics | Body hair | Gene mutations | Growth | Proteus syndrome | Histones | Hypertrichosis | Causes of | Genetic aspects | Research | Diagnosis | Health aspects | Proteins | Genotype & phenotype | Genetic disorders | Mutation | Mental disorders | Index Medicus | Hair | Enzymes | Body height | MLL protein | histone methyltransferase | Transcription | Catalysis | Methylation | Elbow | Mental retardation | Report
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7. Prevalence of fetal alcohol spectrum disorders in 4 US communities
by May, Philip A and Chambers, Christina D and Kalberg, Wendy O and Zellner, Jennifer and Feldman, Haruna and Buckley, David and Kopald, David and Hasken, Julie M and Xu, Ronghui and Honerkamp-Smith, Gordon and Taras, Howard and Manning, Melanie A and Robinson, Luther K and Adam, Margaret P and Abdul-Rahman, Omar and Vaux, Keith and Jewett, Tamison and Elliott, Amy J and Kable, Julie A and Akshoomoff, Natacha and Daniel, Falk and Arroyo, Judith A and Hereld, Dale and Riley, Edward P and Charness, Michael E and Coles, Claire D and Warren, Kenneth R and Jones, Kenneth Lyons and Hoyme, H. Eugene
JAMA : the journal of the American Medical Association, ISSN 0098-7484, 02/2018, Volume 319, Issue 5, pp. 474 - 482
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | United States - epidemiology | Prevalence | Cross-Sectional Studies | Humans | Child, Preschool | Male | Mothers | Sampling Studies | Socioeconomic Factors | Fetal Alcohol Spectrum Disorders - epidemiology | Adult | Female | Fetal Alcohol Spectrum Disorders - ethnology | Child | Fetal alcohol syndrome | Communities | Parents | Disorders | Disabilities | Life assessment | Exposure | Neurodevelopmental disorders | Estimates | Children & youth | Disability | Pregnancy | Alcoholic beverages | Children | Sampling | Prenatal experience
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8. Full Text Bone Marrow-Harvesting Technique Influences Functional Heterogeneity of Mesenchymal Stem/Stromal Cells and Cartilage Regeneration
by Sivasubramaniyan, K and Ilas, D.C and Harichandan, A and Bos, Koen and Santos, D.L and de Zwart, P and Koevoet, Wendy J.L.M and Owston, H and Bühring, H.-J and Jones, E and Osch, Gerjo
The American journal of sports medicine, ISSN 0363-5465, 12/2018, Volume 46, Issue 14, pp. 3521 - 3531
chondrogenic ability | cartilage injuries | cell therapy | stem cell heterogeneity | Sport Sciences | Life Sciences & Biomedicine | Orthopedics | Science & Technology | Osteogenesis - physiology | Cartilage Diseases | Cell Count | Humans | Middle Aged | Mesenchymal Stem Cells - physiology | Bone Marrow Cells - physiology | Male | Receptors, Nerve Growth Factor - metabolism | Bone Marrow - physiology | Flow Cytometry | Leukocyte Common Antigens - physiology | Ilium - surgery | Bone Marrow Transplantation | Aged, 80 and over | Cartilage - physiology | Female | Cell Differentiation | Tissue and Organ Harvesting - methods | Regeneration - physiology | Nerve Tissue Proteins - metabolism | Chondrogenesis - physiology | Stem Cells - physiology | Aged | Mesenchymal Stem Cell Transplantation | Cartilage - injuries | Index Medicus
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