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1-141 out of 141 article(s)
Title Author Type Date Words
Novel MTTP Gene Mutation in a Case of Abetalipoproteinemia with Central Hypothyroidism. Ustkoyuncu, Pembe Soylu; Gokay, Songul; Eren, Esra; Dogan, Durmus; Yildiz, Gokce; Yilmaz, Aysegul; M Clinical report Dec 1, 2020 2611
Sidra uses precision medicine to treat rare diseases in children. Nov 10, 2020 632
First report of human astrovirus MLB2 in Brazil detected in feces of children with acute gastroenteritis living in the state of Roraima, Northern Brazil. Olivares, Alberto Ignacio Olivares; de Moraes, Marcia Terezinha Baroni; de Queiroz, Herika Caroline Report Nov 1, 2020 3007
Autoinflammatory Diseases in Childhood. Yildiz, Mehmet; Haslak, Fatih; Adrovic, Amra; Barut, Kenan; Kasapcopur, Ozgur Sep 1, 2020 8432
Role of Colchicine Treatment in Tumor Necrosis Factor Receptor Associated Periodic Syndrome (TRAPS): Real-Life Data from the AIDA Network. Vitale, Antonio; Sota, Jurgen; Obici, Laura; Ricco, Nicola; Maggio, Maria Cristina; Cattalini, Marco Jun 30, 2020 3746
A Case of Late-onset Hyperinsulinemic Hypoglycemia: HNF4A Mutation. Arslan, Gulcin; Acar, Sezer; Ozdemir, Taha Resid; Nalbantoglu, Ozlem; Kirbiyik, Ozgur; Koprulu, Ozge Jun 1, 2020 2855
Characteristics of Children with Alagille Syndrome at Children's Hospital No. 1, Vietnam. Van Ta, Tram; Nguyen, Truong Viet; Pham, Hien The; Nguyen, Tuan Anh Report Jan 1, 2020 2567
Etiological Study of Various Retinal Diseases in Paediatric Population at a Tertiary Eye Centre, Telangana State. Sultana, Aliya; Hyndavi, Bellaganti Nov 25, 2019 4052
The Spectrum of MEFV Gene Mutations and Genotypes in the Middle Northern Region of Turkey. Celep, Gokce; Durmaz, Zeynep Hulya; Erdogan, Yalciner; Akpinar, Seviye; Kaya, Saban Abdullah; Guckan Oct 1, 2019 4750
Genotype-phenotype Correlation in Pelizaeus Merzbacher Disease and Pelizaeus Merzbacher-like Disease. Gokcal, Elif; Bilir, Birdal; Battaloglu, Esra; Aydin, Resa; Yapici, Zuhal Jul 1, 2019 3578
HLA Haplotype Association with Celiac Disease in Albanian Pediatric Patients from Kosovo. Ramosaj-Morina, Atifete; Kamenaric, Marija Burek; Azemi, Mehmedali; Spahiu, Lidvana; Grubic, Zorana; Jun 30, 2019 5784
Abernethy malformation. Mehra, Shibani; Walia, Sonam; Karthikeyan, M.A.; Garga, U.C. Dec 1, 2018 1539
PTC Therapeutics Presents Initial Data from Patient Registry Demonstrating Translarna Slows Disease Progression in Children with Duchenne Caused by a Nonsense Mutation. Oct 8, 2018 979
A Novel De Novo Missense Mutation in HNF4A Resulting in Sulfonylurea-Responsive Maturity-onset Diabetes of the Young. Acar, Sezer; Abaci, Ayhan; Demir, Korcan; Ozdemir, Taha Resid; Ozyilmaz, Berk; Bober, Ece Clinical report Sep 1, 2018 2332
A Rare Case of Cholestasis: Arthrogryposis, Renal Tubular Disorder and Cholestasis Syndrome. Turkmenoglu, Yelda; Acar, Yesim; Ozdemir, Fatih Cemal; Singer, Ralfi; Berdeli, Afig; Adal, Servet Er Clinical report Sep 1, 2018 1799
Association between serotonin 2C receptor gene (HTR2C) polymorphisms and psychopathological symptoms in children and adolescents. Paes, L.A.; Torre, O.H. Della; Henriques, T.B.; de Mello, M.P.; Celeri, E.H.R.V.; Dalgalarrondo, P.; Report Aug 1, 2018 4025
New genes linked to childhood nephrotic syndrome identified. Jul 29, 2018 291
A rare cause of sudden cardiac arrest: Catecholaminergic polymorphic ventricular tachycardia. Atik, Sezen Ugan; Alp, Firuze Erbek; Dedeoglu, Reyhan; Koka, Aida; Oztunc, Funda; Eroglu, Ayse Guler Clinical report Jun 1, 2018 2195
Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation. Cakir, Aydilek Dagdeviren; Turan, Hande; Aykut, Ayca; Durmaz, Asude; Ercan, Oya; Evliyaoglu, Olcay Report Jun 1, 2018 2826
The kids are too clean! Germ-free environment in first year of childhood linked to LEUKAEMIA, claims study; Overly sterile environments for young children can be a major factor behind childhood leukaemia according to doctors. May 21, 2018 900
EVALUATION OF TREATMENT MODALITIES OF CONGENITAL NASOLACRIMAL DUCT OBSTRUCTION IN PAEDIATRIC PATIENTS FROM A TERTIARY EYE CARE CENTRE. Kai, Sanjay; Raina, Bhavani; Sharma, Pallavi Report May 7, 2018 2553
Clinical and mutational spectrum of Colombian patients with Pelizaeus Merzbacher Disease/Heterogeneidad clinica y mutacional en pacientes colombianos con Pelizaeus Merzbacher. Parra, Harvy Mauricio Velasco; Anaya, Silvia Juliana Maradei; Guio, Johanna Carolina Acosta; Diaz, C Apr 1, 2018 4064
Risk of Secondary ADHD Higher After Childhood TBI; Severe traumatic brain injury increases SADHD risk; within TBI group, familial dysfunction ups risk. Mar 19, 2018 291
Early-Onset Isolated Bilateral Pheochromocytoma As a Major Clinical Manifestation of von-Hippel Lindau Syndrome Type 2C. Acar, Sezer; Tuhan, Hale; Demir, Korcan; Aykut, Ayca; Durmaz, Asude; Karaarslan, Unal Utku; Inci, Go Clinical report Mar 1, 2018 2484
Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia. Arif, Tasleem; Adil, Mohammad; Amin, Syed Suhail Case study Jan 1, 2018 1217
Latest Insights on the Etiology and Management of Primary Adrenal Insufficiency in Children. Guran, Tulay Report Dec 1, 2017 7944
Congenital Hyperinsulinism: Diagnosis and Treatment Update. Demirbilek, Huseyin; Hussain, Khalid Report Dec 1, 2017 14555
Dysmorphic Features, Frontal Cerebral Cavernoma, and Hyperglycemia in a Girl with a De Novo Deletion of 7.23 Mb in Region 7p13-p12.1. Lopez, Gilberto Perez; Quispe, Beatriz Villafuerte; Nunez, Maria Jose Cabrejas; Castano, Luis; Barri Case study Dec 1, 2017 2859
Interleukin-6 and Interleukin-17 gene polymorphisms and celiac disease susceptibility. Ecevit, Cigdem Omur Nov 1, 2017 1372
Interleukin-6 and interleukin-17 gene polymorphism association with celiac disease in children. Akbulut, Ulas Emre; Cebi, Alper Han; Sag, Elif; Ikbal, Mevlit; Cakir, Murat Nov 1, 2017 3767
Clinical and Genetic Findings of Turkish Hypophosphatasia Cases. Saglam, Halil; Erdol, Sahin; Dorum, Sevil Report Sep 1, 2017 5692
PROP1-Related Combined Pituitary Hormone Deficiency: Case Report. Paketci, Ahu; Acar, Sezer; Demir, Korcan; Abaci, Ayhan; Bober, Ece Case study Jun 1, 2017 348
Schmid Type of Metaphyseal Chondrodysplasia with COL10A1 Mutation. Cimbek, Emine Ayca; Sen, Yasar; Sen, Askin; Yuca, Sevil Ari; Bugrul, Fuat Brief article Jun 1, 2017 188
Thyroid Hormone Resistance P453A Mutation. Ugurlu, Aylin Kilinc; Doger, Esra; Akbas, Emine Demet; Bideci, Aysun; Camurdan, Orhun; Cinaz, Peyami Case study Jun 1, 2017 313
A Case of Vanishing Testis Syndrome. Korkmaz, Huseyin Anil Case study Jun 1, 2017 278
A Novel Mutation in AMHR2 Gene in Two Siblings with Persistent Mullerian Duct Syndrome. Cakir, Aydilek Dagdeviren; Turan, Hande; Tuysuz, Beyhan; Onay, Huseyin; Ercan, Oya; Evliyaoglu, Saad Report Jun 1, 2017 321
HOXC4 Gene is Possibly Responsible for Lin-Gettig Syndrome. Atik, Tahir; Isik, Esra; Ozen, Samim; Akgun, Bilcag; Onay, Huseyin; Cogulu, Ozgur; Erguner, Bekir; S Case study Jun 1, 2017 319
A Novel THRA Gene Mutation in Patient with Thyroid Hormone Resistance. Korkmaz, Ozlem; Ozen, Samim; Ozdemir, Taha Resid; Goksen, Damla; Darcan, Sukran Case study Jun 1, 2017 353
Nonoperative management of neglected clubfoot--our experience. Babu, P. Anil; Prasad, G. Vara Report May 18, 2017 2455
Small-magnitude effect sizes in epigenetic end points are important in children's environmental health studies: the children's environmental health and disease prevention research center's epigenetics working group. Breton, Carrie V.; Marsit, Carmen J.; Faustman, Elaine; Nadeau, Kari; Goodrich, Jaclyn M.; Dolinoy, Report Apr 1, 2017 18222
Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy. Su, Xueying; Lin, Ruizhu; Huang, Yonglan; Sheng, Huiying; Li, Xiaofei; Ting, Tzer Hwu; Liu, Li; Li, Report Mar 1, 2017 3918
A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene. Keskin, Meliksah; Sahin, Nursel Muratoglu; Kurnaz, Erdal; Bayramoglu, Elvan; Erdeve, Senay Savas; Ay Case study Mar 1, 2017 2382
Preoperative Serum IL-12p40 Is a Potential Predictor of Kasai Portoenterostomy Outcome in Infants with Biliary Atresia. Goda, Shaimaa Samy; Khedr, Mohamed Ahmed; Elshenawy, Soha Zaki; Ibrahim, Tarek Mohamed; Araby, Hanaa Report Jan 1, 2017 5607
Association of Polymorphisms in Toll-Like Receptors 4 and 9 with Autoimmune Thyroid Disease in Korean Pediatric Patients. Cho, Won Kyoung; Jang, Jung-Pil; Choi, Eun-Jeong; Ahn, Moonbae; Kim, Shin Hee; Cho, Kyoung Soon; Par Report Jan 1, 2017 5410
Environmental risk factors and acute lymphoblastic leukaemia in childhood/Factores de riesgo ambientales y leucemia linfoblastica aguda en la infancia/Fatores de risco ambientais e leucemia linfoblastica aguda na infancia. Pereira, Fernanda Alves Cangerana; Mirra, Antonio Pedro; de Oliveira Latorre, Maria do Rosario Dias; Jan 1, 2017 6861
Biochemical and Molecular Analysis of the Hb Lepore Boston Washington in a Syrian Homozygous Child. Pirastru, Monica; Manca, Laura; Trova, Sandro; Mereu, Paolo Clinical report Jan 1, 2017 3765
Prevalence of Helicobacter pylori vacA Genotypes and cagA Gene in Dental Plaque of Asymptomatic Mexican Children. Mendoza-Cantu, Alejandra; Urrutia-Baca, Victor Hugo; Urbina-Rios, Cynthia Sofia; De la Garza-Ramos, Report Jan 1, 2017 7898
Urinary Exosomal miR-193a Can Be a Potential Biomarker for the Diagnosis of Primary Focal Segmental Glomerulosclerosis in Children. Huang, Zhibin; Zhang, Yong; Zhou, Jianhua; Zhang, Yu Report Jan 1, 2017 3699
Inherited Paediatric Motor Neuron Disorders: Beyond Spinal Muscular Atrophy. Teoh, Hooi Ling; Carey, Kate; Sampaio, Hugo; Mowat, David; Roscioli, Tony; Farrar, Michelle Report Jan 1, 2017 14930
Nonfamilial Juvenile Polyposis Syndrome with Exon 5 Novel Mutation in SMAD 4 Gene. Ahmed, Amna; Alsaleem, Badr Clinical report Jan 1, 2017 1082
Systemic Pseudohypoaldosteronism Type I: A Case Report and Review of the Literature. Nur, Nasifa; Lang, Cameron; Hodax, Juanita K.; Quintos, Jose Bernardo Clinical report Jan 1, 2017 5083
Cross-sectional analysis of progressive familial intrahepatic cholestasis in Puerto Rican children. Soler, Dellys M.; Del Valle, Antonio I.; Fernandez-Lube, David; Shneider, Benjamin L. Survey Dec 1, 2016 2582
NIH discovers new children's disease. Oct 1, 2016 314
Endocrine Dysfunctions in Patients with Inherited Metabolic Diseases. Erdol, Sahin; Saglam, Halil Report Sep 1, 2016 2778
Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism. Guven, Ayla; Cebeci, Ayse Nurcan; Ellard, Sian; Flanagan, Sarah E. Report Jun 1, 2016 5698
Averting the legacy of kidney disease focus on childhood. Ingelfinger, J.R.; Kalantar-Zadeh, K.; Schaefer, F. Report May 1, 2016 4360
Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis. Liu, Shiguo; Chai, Jian; Zheng, Guohua; Li, Huichao; Lu, Deguo; Ge, Yinlin Report Mar 1, 2016 3054
Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome. Vuralli, Dogus; Gonc, Nazli; Vidaud, Dominique; Ozon, Alev; Alikasifoglu, Ayfer; Kandemir, Nurgun Case study Mar 1, 2016 3626
Averting the Legacy of Kidney Disease-Focus on Childhood. Ingelfinger, Julie R.; Kalantar-Zadeh, Kamyar; Schaefer, Franz Editorial Mar 1, 2016 4471
Assessment of tumors in children with tuberous sclerosis: a single centre's experience. Emir, Suna; Hacisalihoglu, Sadan; Ozyoruk, Derya; Ekici, Filiz; Degerliyurt, Aydan; Guven, Alev; Cet Report Mar 1, 2016 3140
Oxidative Stress in Cancer-Prone Genetic Diseases in Pediatric Age: The Role of Mitochondrial Dysfunction. Perrone, Serafina; Lotti, Federica; Geronzi, Ursula; Guidoni, Elisa; Longini, Mariangela; Buonocore, Jan 1, 2016 6056
Importance of early and multidisciplinary intervention in patients with coexistent juvenile idiopathic arthritis and Familial Mediterranean fever/Juvenil idiopatik artrit ve Ailesel Akdeniz Atesi birlikteliginde erken tedavi ve multidisipliner yaklasimin onemi. Ozen, Selin; Gok, Haydar; Kutlay, Sehim Report Sep 1, 2015 1901
Rotavirus epidemiology in Bangui, Central African Republic, 2008. Gouandijka-Vasilache, Ionela; Manirakiza, Alexandre; Gody, Jean Chrysostom; Banga-Mingo, Virginie; K Report Jul 1, 2014 1431
Association of X4 tropism with disease progression in antiretroviral-treated children and adolescents living with HIV/AIDS in Sao Paulo, Brazil. Almeida, Flavia Jacqueline; Zaparoli, Mayra Simioni; Moreira, Denise Helena; Cavalcanti, Jaqueline d Report May 1, 2014 6721
Pediatric within-day biological variation and quality specifications for 38 biochemical markers in the CALIPER cohort. Bailey, Dana; Bevilacqua, Victoria; Colantonio, David A.; Pasic, Maria D.; Perumal, Nandita; Chan, M Report Mar 1, 2014 8976
Rare childhood disease holds clues for others. Feb 1, 2014 364
Evidence of vaccine-related reassortment of rotavirus, Brazil, 2008-2010. Rose, Tatiana Lundgren; da Silva, Marcelle Figueira Marques; Gomez, Mariela Martinez; Resque, Hugo R Report Nov 1, 2013 2842
Human bocavirus in children with acute gastroenteritis, Chile, 1985-2010. Levican, Jorge; Navas, Esteban; Orizola, Joaquin; Avendaho, Luis Fidel; Gaggero, Aldo Report Nov 1, 2013 2086
Value of real-time polymerase chain reaction in bronchoalveolar lavage fluid for diagnosis of pediatric pulmonary tuberculosis. Wang, Xinfeng; Wu, Yan Hua; Zhang, Kaihui; Guan, Cuiping; Gao, Xusheng; Wang, Maoshui Letter to the editor Nov 1, 2013 1160
Relationship between genetic mutation variations and acute-phase reactants in the attack-free period of children diagnosed with familial Mediterranean fever. Kosan, C.; Cayir, A.; Turan, M.I. Report Oct 1, 2013 2484
Cause of severe seizures in children. Oct 1, 2013 319
Comparison of oral microflora in selective IgA deficiency and X linked agammaglobulinemia cases with control group/Selektif IgA eksikligi ve X'e bagli agammaglobulinemi olgularinda agiz mikroflorasinin saglam grupla karsilastirilmasi. Kiykim, Ayca Aslan; Topcuoglu, Nursen; Kulekci, Guven; Cokugras, Haluk; Akcakaya, Necla; Camcioglu, Report Sep 1, 2013 4048
Balance and self-efficacy of balance in children with CHARGE syndrome. Haibach, Pamela S.; Lieberman, Lauren J. Report Jul 1, 2013 6041
Genes may make kids picky eaters. Brief article Jun 1, 2013 258
Cerebral venous thrombosis associated with childhood ulcerative colitis. Kutluk, Gunsel; Hacifazlioglu, Nilufer Eldes; Horozoglu, Hilal; Ertem, Deniz; Yilmaz, Yuksel Case study Jun 1, 2013 3319
MicroRNAs in idiopathic childhood nephrotic syndrome. Lorenzen, Johan M.; Thum, Thomas Editorial Apr 1, 2013 2320
Increased serum and urinary microRNAs in children with idiopathic nephrotic syndrome. Luo, Yang; Wang, Cheng; Chen, Xi; Zhong, Tianying; Cai, Xiaoyi; Chen, Sidi; Shi, Yonghui; Hu, Jing; Report Apr 1, 2013 5691
How does mom's nutrition affect her children's health? Epigenetics may provide new insights. Wood, Marcia Mar 1, 2013 1071
Pharmacogenomics in children: advantages and challenges of next generation sequencing applications. Vanakker, O.M.; De Paepe, A. Jan 1, 2013 5924
Correlation between PPAR gene polymorphisms and primary nephrotic syndrome in children. Jin, Jiaping; Ding, Guixia; Bao, Huaying; Chen, Ying; Han, Yuan; Zhao, Fei; Huang, Songming; Zhang, Report Jan 1, 2013 5838
Beyond morphology: unraveling the genetic basis of childhood nephrotic syndrome in Pakistan. Mubarak, Muhammed; Kazi, Javed I. Report Nov 30, 2012 1346
Novel human enterovirus C infection in child with community-acquired pneumonia. Daleno, Cristina; Piralla, Antonio; Usonis, Vytautas; Scala, Alessia; Ivaskevicius, Rimvydas; Baldan Letter to the editor Nov 1, 2012 1341
The public health and policy implications of epigenetics and pediatric health research. Witherspoon, Nsedu Obot; Trousdale, Kristie; Bearer, Cynthia F.; Miller, Rachel L. Editorial Oct 1, 2012 1765
'If it's only a blood test, which isn't very traumatic, why not?' Exploring predictive genetic testing in adoption. Dewell, Celia Report Sep 22, 2012 1958
Naturopathic management of infections of the heart and their sequelae. Mikolai, Jeremy; Wilner, Martin Clinical report May 1, 2012 8207
Childhood cancer survivors' children. Brief article Mar 1, 2012 122
Behavioral problems of encopretic children and their familial characteristics/Enkoprezisi olan cocuklarda davranis sorunlari ve bazi ailesel ozellikler. Demir, Turkay; Yavuz, Mesut; Dogangun, Burak; Bolat, Nurullah; Kadak, Tayyib; Karacetin, Gul; Kayaal Report Mar 1, 2012 2936
We can slow the process; Scientists find new therapy to fight ageing. Nov 2, 2011 556
Astrovirus MLB2 viremia in febrile child. Holtz, Lori R.; Wylie, Kristine M.; Sodergren, Erica; Jiang, Yanfang; Franz, Carl J.; Weinstock, Geo Report Nov 1, 2011 1900
NIH scientists discover link among spectrum of childhood diseases. Oct 31, 2011 110
Gene responsible for three forms of childhood neurodegenerative diseases found. Sep 15, 2011 344
Children and genetic identification of talent. Inoue, Yusuke; Muto, Kaori Report Sep 1, 2011 649
Polycyclic aromatic hydrocarbons-aromatic DNA adducts in cord blood and behavior scores in New York City Children. Perera, Frederica P.; Wang, Shuang; Vishnevetsky, Julia; Zhang, Bingzhi; Cole, Kathleen J.; Tang, De Report Aug 1, 2011 7109
Immunoglobulin light chain levels can be used to determine disease stage in children with juvenile idiopathic arthritis. Kutulculer, Necil; Karaca, Neslihan E.; Azarsiz, Elif; Aksu, Guzide; Gulez, Nesrin Report Mar 22, 2011 3498
Genetic screening of prospective parents. Murray, Michael F. Feb 15, 2011 777
Reprogenetics and the "parents have always done it" argument. Malmqvist, Erik Jan 1, 2011 5134
Enterovirus 75 encephalitis in children, Southern India. Lewthwaite, Penny; Perera, David; Ooi, Mong How; Last, Anna; Kumar, Ravi; Desai, Anita; Begum, Ashia Report Nov 1, 2010 2132
The genetics of mental illness: a guide for parents and adoption professionals. Uher, Rudolf Sep 22, 2010 2015
A case of Lujan-Fryns syndrome/ Lujan-Fryns sendromlu bir olgu sunumu. Dundar, Nihal Olgac; Dundar, Bumin Nuri; Akkaya, Ayca Esra Case study Sep 1, 2010 1220
Clinical and molecular-genetic investigation of non-syndromic hearing disorders in children of the Uzbek population. Khushvakova, Nilufar Report Apr 1, 2010 2090
Child health vow. Jan 10, 2010 371
Circadian clock genes linked to bipolar disorder in children. Mechcatie, Elizabeth Jan 1, 2010 281
Genetic characteristic of non-syndromal neurosensory children's hearing loss in Uzbek population. Khushvakova, Nilufar; Mukhamedov, Rustam; Hakimov, Abdumalik Report Jan 1, 2010 1374
Faulty body clock genes could cause bipolar disorder in kids. Nov 12, 2009 308
Pediatric points. Roy-Bornstein, Carolyn Nov 1, 2009 622
Gluten-free diet lessens bone problems in kids with celiac disease. Oct 21, 2009 285
Gluten-free diet lessens bone problems in kids with celiac disease. Oct 12, 2009 283
Too much TV, computer screen time can up high BP risk in kids. Aug 4, 2009 379
2009. Calendar Aug 1, 2009 2565
Diabetes gene predisposes kids to have lower birth weight. Jul 30, 2009 385
Recruitment gets started for National Children's Study. Schneider, Mary Ellen Brief article Jun 1, 2009 243
Healthy diet can offset 'obesity gene' in kids. Mar 4, 2009 422
Unrelated cord blood transplantation helps children with deadly conditions. Mar 1, 2009 274
Study rules out link between smoking in pregnancy and anti-social children. Feb 3, 2009 293
Study rules out link between smoking in pregnancy and anti-social children. Feb 3, 2009 292
Gene linked to obesity in children; HEALTH. Jan 12, 2009 126
Gene linked to obesity in children; HEALTH. Jan 12, 2009 126
Human gene mutations expressed in yeast may predict severity of fatal childhood illness. Dec 22, 2008 246
Increased C3-carnitine in a healthy premature infant. Chapman, Kimberly A.; Bennett, Michael J.; Sondheimer, Neal Nov 1, 2008 3286
Behavioral phenotype helps diagnose FASD in children. Splete, Heidi Aug 1, 2008 538
Cirrhosis originally diagnosed as nonalcoholic steatohepatitis. Snyder, Marion L.; Fantz, Corinne R. Aug 1, 2008 3521
Genetic clue to obese children; In association with the NHS. Jul 21, 2008 138
Is asthma dangerous? Ask Alan YOUR CHILD HEALTH QUERIES. May 27, 2008 179
Fit or flabby future; Lifelong study of children to see if diet gives them ... Jan 29, 2008 709
Target obesity in kids with genetic syndromes: reserve medications for those with genetic conditions such as familial hypercholesterolemia. Bates, Betsy Jan 15, 2008 699
Your LIFE: EVEN FIT KIDS ARE AT RISK; HEALTH STORIES. Dec 21, 2007 158
National Children's Study centers picked. Arias, Donya C. Brief article Dec 1, 2007 205
Omega-3 fats may cut risk of diabetes in at-risk kids. Moon, Mary Ann Clinical report Oct 1, 2007 378
Norovirus detection and genotyping for children with gastroenteritis, Brazil. Soares, Caroline C.; Santos, Norma; Beard, Rachel Suzanne; Albuquerque, Maria Carolina M.; Maranhao, Aug 1, 2007 2204
Genetic basis likely behind pediatric psoriasis. Johnson, Kate Aug 1, 2007 609
Growth hormone (GH) receptor isoform in acromegaly: lower concentrations of GH but not insulin-like growth factor-I in patients with a genomic deletion of exon 3 in the GH receptor gene. Schmid, Christoph; Krayenbuehl, Pierre-Alexandre; Bernays, Rene-Ludwig; Zwimpfer, Cornelia; Maly, Fr Aug 1, 2007 3329
Gene CYP2D6 and risperidone. Brief article Mar 1, 2007 217
When should we screen children for hyperlipidemia? Misicko, Nancy E.; St Anna, Leilani Aug 1, 2006 1231
Children conceived by sperm donation: attitudes to their right to know. Nov 1, 2005 360
Keeping families in once they've come through the door: attrition in parent-child interaction therapy. Fernandez, Melanie A.; Eyberg, Sheila M. Sep 22, 2005 2800
For the small number of children who have only one copy of a gene variant that regulates a crucial brain messenger chemical, the chances of schizophrenia rise significantly. Brief article Jun 22, 2005 181
Parental atopy increases risk in children. Johnson, Kate Brief Article Jun 1, 2005 303
The gene scene: generating interest in biotech. Schwarcz, Joe Feb 1, 2005 925
The Impact of Technology Use on Low-Income and Minority Students' Academic Achievements: Educational Longitudinal Study of 2002. Du, Janxia; Sansing, William; Yu, Chien Abstract Oct 1, 2004 247
DNA sample program seeks bank sponsors. (Marketing News). Brief Article Nov 1, 2002 92
Total homocysteine in pediatric patients. Vilaseca, M. Antonia; Moyano, Dolores; Ferrer, Imma; Artuch, Rafael Apr 1, 1997 1558

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