Care and treatment subtopic
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Articles
1-94 out of 94 article(s)
| Title |
Author |
Type |
Date |
Words |
| Blood disease centre on way. |
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Jan 19, 2013 |
314 |
| Grifols Announces First Patient Enrolled and Dosed in Phase II Trial of Alpha-1 HC Aerosol to Treat Cystic Fibrosis. |
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Oct 8, 2012 |
590 |
| Grifols Announces First Patient Enrolled and Dosed in Phase II Trial of Alpha-1 HC Aerosol to Treat Cystic Fibrosis. |
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Clinical report |
Oct 8, 2012 |
609 |
| Boston Children's surgeons pilot expandable prosthetic valves for children with congenital heart disease. |
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Oct 3, 2012 |
1165 |
| BioRx Receives Limited Distribution Rights to Corifact[R] for the Treatment of Congenital Factor XIII Deficiency. |
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Jul 11, 2012 |
603 |
| Effect of locally made ready-to-use therapeutic food (Mushpro Health Drink Powder--MHDP) for treatment of malnutrition on children aged 6 to 72 months in tribal area of Amravati District of Maharashtra, India: a randomized control trial. |
Wasnik, Vinod R.; Rathi, Manoj |
Report |
Jul 1, 2012 |
3769 |
| Palestinian girl gets treatment for rare eye disease in Dubai. |
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Jun 25, 2012 |
1167 |
| Third Rock Ventures Launches Global Blood Therapeutics with $40.7 Million to Revolutionize the Treatment of Chronic Blood-Based Diseases. |
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Jun 14, 2012 |
1298 |
| Three -way IVF 'ethical" says report; Treatment tackles genetic disorders. |
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Jun 12, 2012 |
462 |
| The University of Cape Town's contribution to medical genetics in Africa--from the past into the future. |
Beighton, P.; Fieggen, K.; Wonkam, A.; Ramesar, R.; Greenberg, J. |
Report |
Jun 1, 2012 |
2640 |
| Poor dental hygiene puts congenital heart disease patients at endocarditis risk. |
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Mar 17, 2012 |
637 |
| New Molecule Has Potential to Help Treat Genetic Diseases and HIV. |
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Feb 15, 2012 |
695 |
| A case of congenital fistula from an accessory parotid gland: diagnosis and treatment. |
Pinto, Fabio Roberto |
Case study |
Jan 1, 2012 |
1502 |
| NHGRI broadens sequencing program focus on inherited diseases, medical applications. |
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Brief article |
Dec 6, 2011 |
124 |
| Whence come treatments for genetic disorders? |
Chandrasek, Niranjana; Edelson, Vaughn; Terry, Sharon F. |
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Dec 1, 2011 |
1093 |
| Young heart patients get free treatment. |
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Oct 27, 2011 |
602 |
| Congenital fixation of the head of the stapes in three family members. |
Wetmore, Stephen J.; Gross, Andrew F.L. |
Clinical report |
Aug 1, 2011 |
2290 |
| Case report: infantile systemic hyalinosis: a dental perspective. |
Olczak-Kowalczyk, D.; Krasuska-Stawinska, E.; Rokicki, D.; Pronicki, M. |
Report |
Aug 1, 2011 |
2004 |
| Mount Sinai Opens New Adult Congenital Heart Disease Clinic. |
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May 5, 2011 |
656 |
| Combination Therapy Provides Hope for Cure of Dangerous Infections of Cystic Fibrosis Patients. |
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Apr 25, 2011 |
441 |
| Blood-clotting agent can be used to diagnose fatal genetic diseases. |
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Feb 4, 2011 |
418 |
| Congenital total absence of pericardium in a patient with left lung lower lobe bronchiectasis/ Sol akciger alt lob bronsektazisi olan bir hastada konjenital total perikart yoklugu. |
Sivrikoz, Muammer Cumhur; Durceylan, Erhan; Boztepe, Hacer; Birdane, Alparslan |
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Feb 1, 2011 |
1221 |
| AMT to Supply cGMP Manufacturing to Consortium Led by Institut Pasteur for Clinical Development of Gene Therapy for Rare Genetic Disorder in Children. |
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Jan 10, 2011 |
1443 |
| AMT to Supply cGMP Manufacturing to Consortium Led by Institut Pasteur for Clinical Development of Gene Therapy for Rare Genetic Disorder in Children. |
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Jan 10, 2011 |
1445 |
| The outcomes of lacrimal massage or probing treatments at early and late ages for congenital nasolacrimal duct obstruction / Dogumsal nazolakrimal kanal tikanikliginda erken ve gec yaslarda uygulanan lakrimal kanal masaj ve sondalama tedavisinin sonuclari. |
Caglar, Cagatay; Batur, Muhammed; Yasar, Tekin; Cinal, Adnan |
Report |
Dec 1, 2010 |
4497 |
| Beware the bifid rib! |
Scheepers, Shaun; Andronikou, Savvas |
Clinical report |
Dec 1, 2010 |
531 |
| A novel way to create stem cells from skin reduces the risk of cancer caused by the original method and may open the way to treatments for genetic diseases. Harvard Stem Cell Institute. |
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Oct 4, 2010 |
332 |
| Case report: rehabilitation of a child with dentinogenesis imperfecta and congenitally missing lateral incisors. |
Millet, C.; Viennot, S.; Duprez, J.P. |
Case study |
Oct 1, 2010 |
3005 |
| NATURE Publishes Promising Results on Treatment of First Patient in bluebird bio's Phase 1/2 Beta-Thalassemia Study. |
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Sep 15, 2010 |
1241 |
| Winning the battle against pseudomonas aeruginosa endocarditis: a case report/Pseudomonas aeruginosa endokarditine karsi savasi kazanmak: vaka sunumu. |
Parlakay, Aslinur Ozkaya; Kara, Ates; Celik, Istemihan; Cengiz, Ali Bulent; Karagoz, Tevfik; Devrim, |
Case study |
Sep 1, 2010 |
1706 |
| After 30 Years, "PeSa Procedure" Remains Best Treatment for Most Congenital Colorectal Conditions. |
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Aug 11, 2010 |
674 |
| Exceptional family TV: The one in a billion genetic condition. |
Charlan, Nathan |
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Aug 1, 2010 |
910 |
| Recommendations for expensive treatments made for a genetic disorder called alpha-1 antitrypsin deficiency should be withdrawn because the drugs have no benefit, scientists said. |
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Jul 12, 2010 |
283 |
| Congenital epulis. |
Bewley, Arnaud; Bloom, Jason D.; Kherani, Safeena; Pawel, Bruce R. |
Clinical report |
Jul 1, 2010 |
768 |
| Multimodality imaging and interventional management of a complex congenital vascular malformation. |
Ahmed, Aadil |
Case study |
Jun 1, 2010 |
1053 |
| The classification of renal cystic diseases and other congenital malformations of the kidney and urinary tract. |
Bonsib, Stephen M. |
Report |
Apr 1, 2010 |
9869 |
| Increased nuchal translucency thickness and normal karyotype. |
Cilliers, J.B.F. |
Brief article |
Apr 1, 2010 |
343 |
| Late referrals, the Fetal Medicine specialist's nightmare. |
de Coning, L. |
Brief article |
Apr 1, 2010 |
122 |
| Medtronic's Melody may be music to some heart defect patients' ears. |
Sohn, Tim |
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Apr 1, 2010 |
1302 |
| New treatment for genetic condition. |
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Brief article |
Mar 26, 2010 |
135 |
| Genetic Disorders Sourcebook, fourth edition. |
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Brief article |
Mar 1, 2010 |
83 |
| Developmental anterior dislocation of the radial head resulting from a congenital solitary osteochondroma of the proximal ulna in an infant. |
Garcia-Mata, Serafin; Hidalgo-Ovejero, Angel M. |
Case study |
Jan 1, 2010 |
2498 |
| Living healthy in the UAE for years to come. |
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Dec 2, 2009 |
634 |
| Results of American Hospital newborn hearing screening program/Amerikan Hastanesi yenidogan isitme taramasi sonuclari. |
Kayiran, Sinan Mahir; Genc, Erkhan; Erdil, Aysen; Gurakan, Berkan A. |
Clinical report |
Dec 1, 2009 |
2214 |
| Lamellar ichtyosis: case report/ Lameller iktiyoz: olgu sunumu. |
Gunduz, Kamer; Kayhan, Tuba Celebi; Gencoglan, Gulsum; Inanir, Isil; Temiz, Peyker |
Author abstract |
Dec 1, 2009 |
1402 |
| Case series: treatment considerations in x-linked hypohidrotic ectodermal dysplasia. |
Lexner, M.O.; Almer, L. |
Report |
Dec 1, 2009 |
3206 |
| Bilateral congenital trigger thumb: a case report and discussion of management. |
Schessler, Matthew J.; McClellan, W. Thomas |
Case study |
Nov 1, 2009 |
1225 |
| FDA Panel Recommends Approval of Medtronic Heart Valve under Humanitarian Device Exemption. |
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Jul 22, 2009 |
752 |
| Laryngeal web associated with Simpson-Golabi-Behmel syndrome in a child. |
Agarwal, M.; Sharma, R.; Panda, A.; Gupta, A. |
Clinical report |
Jul 1, 2009 |
596 |
| Revolutionary drug for boy; HEALTH: A rare genetic disorder is treated with enzymes. |
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May 6, 2009 |
388 |
| Revolutionary drug for boy; HEALTH: Children's hospital first to treat rare genetic disorder. |
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May 6, 2009 |
318 |
| Genes, DNA, diet, heredity, and disease. |
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Report |
May 1, 2009 |
1549 |
| Systems to determine treatment effectiveness in newborn screening. |
Howell, R. Rodney |
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Jan 1, 2009 |
3063 |
| On treatability: considerations of treatment in the context of newborn screening. |
Natowicz, Marvin R.; Zuckerman, Shlomit |
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Jan 1, 2009 |
4041 |
| Scientists recreate hallmarks a genetic disorder in lab. |
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Dec 22, 2008 |
462 |
| Should helmets be used for flattened heads? |
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Nov 1, 2008 |
405 |
| An unusual Brugada syndrome case/nadir gorulen bir Brugada sendromu vakasi. |
Orem, Cihan; Kiris, Gulhanim; Durmus, Ismet; Kaplan, Sahin; Gedikli, Omer; Baykan, Merih; Gokce, Mus |
Case study |
Oct 1, 2008 |
1269 |
| A parent's view of Ohdo syndrome. |
FitzZaland, Richard; FitzZaland, Mary |
Clinical report |
Aug 1, 2008 |
1262 |
| Seventh cervical rib associated with subclavian artery occlusion and multiple infarcts: case report. |
Wise, Roxanne |
Case study |
Jun 1, 2008 |
2279 |
| Gene Therapy Improves Vision in Patients with Congenital Retinal Disease. |
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Apr 27, 2008 |
2137 |
| OxThera: Pivotal study is being conducted with Oxabact(TM) for the treatment of Primary Hyperoxaluria. |
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Clinical report |
Apr 3, 2008 |
776 |
| Congenital midline cervical cleft: a report of two cases. |
Franzese, Christine; Hayes, James D.; Nichols, Kristie |
Report |
Mar 1, 2008 |
2064 |
| The Human Genome Project: implications for families. |
Miller, Virginia L.; Martin, Angela M. |
Case study |
Feb 1, 2008 |
2295 |
| How far is too far in enhancing kids' genetic traits? |
Lawton, Kim |
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Sep 21, 2007 |
886 |
| Children's heart disease site keeps eye on all UK centres. |
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Jun 1, 2007 |
651 |
| Long-term follow-up of a multiloculated arachnoid cyst of the middle cranial fossa. |
Kennedy, David W. |
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Jun 1, 2007 |
2759 |
| Medtronic Announces First U.S. Implant of Its Melody Transcatheter Valve for Patients with Congenital Heart Disease. |
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Feb 19, 2007 |
673 |
| Enzo Biochem Announces Plans to Produce Single Copy DNA Probes That Could Open Door to More Effective Treatment of Genetic Diseases and Cancer. |
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May 23, 2006 |
1012 |
| Methylphenidate and cell abnormalities. |
Splete, Heidi |
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May 1, 2006 |
241 |
| ICDs protect young hearts. |
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Brief article |
May 1, 2006 |
139 |
| European Regulatory Committee Recommends Orphan Medicinal Product Designation for Amicus Therapeutics' Amigal(TM) for Fabry Disease. |
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Apr 11, 2006 |
444 |
| Spontaneous transtemporal CSF leakage: a study of 51 cases. |
Vukas, Daniel D. |
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Nov 1, 2005 |
2018 |
| Elliott Gould Narrates New DVD Promoting Awareness of Most Common Genetic Disease Facing U.S. Jews. |
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Oct 20, 2005 |
669 |
| Imaging can match brain structure to behavior. |
MacReady, Norra |
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Feb 1, 2005 |
642 |
| Branchial cleft cyst. |
Thompson, Lester D.R. |
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Nov 1, 2004 |
349 |
| Unraveling the genetics of bipolar disorder. |
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Nov 1, 2004 |
617 |
| GYN/OB-1. Isolated femoral dysplasia is a sonographic manifestation of congenital rickets. |
Royek, Anthony B. |
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Oct 1, 2004 |
309 |
| Millennium obtains United States patent. |
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Sep 1, 2004 |
98 |
| Population-based carrier screening and prenatal diagnosis. |
Strom, Charles M. |
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Aug 1, 2004 |
5200 |
| Does patenting genes change the meaning of life? (Ethical Aspects). |
Thompson, Richard E. |
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May 1, 2003 |
1998 |
| Nicole's answer: Costello syndrome. |
Kim, Arnold |
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May 1, 2003 |
1379 |
| IFOPA: International Fibrodysplasia Ossificans Progressiva Association. (organizational spotlight). |
Hair, Marilyn |
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Nov 1, 2002 |
981 |
| Prader-Willi syndrome. (ask the doctor). |
Butler, Merlin G. |
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Nov 1, 2001 |
753 |
| Hunt for an elusive gene. |
Forstall, Joanne; Forstall, Rob; Cannataro, Jennifer |
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Oct 1, 2001 |
1649 |
| Dura Mater Involvement in Ochronosis (Alkaptonuria). |
Liu, Wendy; Prayson, Richard A. |
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Jul 1, 2001 |
1402 |
| Inhale receives Orphan Designation for inhaleable hereditary emphysema therapy. |
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Brief Article |
Jul 1, 2001 |
746 |
| Questions and answers about heritable disorders of connective tissue. (Health Topics). |
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Pamphlet |
Jul 1, 2001 |
3153 |
| Hereditary angioedema: Report of a case. |
Wormald, Peter J. |
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May 1, 2001 |
870 |
| Milked enzyme thwarts muscle disorder. |
J.T. |
Brief Article |
Nov 4, 2000 |
320 |
| Transplanted Cells May Arrest Genetic Diseases. |
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Brief Article |
Feb 1, 2000 |
401 |
| Single-step mutation scanning of the 6-pyruvoyltetrahydropterin synthase gene in patients with hyperphenylalaninemia. |
Romstad, Anne; Guldberg, Per; Blau, Nenad; Guttler, Flemming |
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Dec 1, 1999 |
4985 |
| The double-edged helix: advances in genetic testing reveal yet another reason we need national health insurance. |
Townsend, Kathleen Kennedy |
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Nov 1, 1997 |
1384 |
| Skin genes underlie blistering disorder. |
Ezzell, Carol |
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Sep 28, 1991 |
575 |
| Cystic fibrosis treatments promising. |
Weiss, Rick |
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Mar 2, 1991 |
735 |
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