... Total and resting energy expenditure in children with sicklecelldiseaseJ Pediatr 2000; 136:73–9 70 Jain SK, Ross JD, Duett J, Herbst JJ Low plasma prealbumin and carotenoid levels in sicklecell ... infants and young children with sicklecelldiseaseJ Am Diet Assoc 2000; 100:330–4 10 Fung EB, Malinauskas BM, Kawchak DA, et al Energy expenditure and intake in children with sicklecelldisease ... are four major genotypes within the definition of SCD: homozygous sicklecell (SS) disease, sickle haemoglobin C (SC) disease, sicklecell bz thalassaemia (S bz thalassaemia) andsicklecell b0...
... Vannatta K, Koontz K, Kalinyak K, Bukowski WM, Davies WH: Peer relationships and emotional well-being of youngsters with sicklecelldisease Child Dev 1996, 67(2):423-436 Barakat LP, Lash LA, Lutz MJ, ... of Children and Adolescents With SickleCellDisease In Comprehensive handbook of childhood cancer andsicklecell disease: A biopsychosocial approach Edited by: Brown RT New York, NY , Oxford ... symptoms in adolescents with sicklecelldiseaseJ Behav Med in press Benton TD, Ifeaqwu JQ, Smith-Whitley K: Anxiety and depression in children and adolescents with sicklecelldisease Curr Psychiatry...
... management of sicklecelldisease N Engl J Med 1995, 333:206-213 Koshy M, Weiner SJ, Miller , Sleeper AL, Vichinsky EP, Brown AK, Khakoo Y, Kinney TR: Surgery and anaesthesia in sicklecelldisease ... Onkologie: Sichelzellkrankheit.http://www.awmf.org Williams TN, Mwangi TW, Wambua S, Alexander ND, Kortok M, Snow RW, Marsh K: Sicklecell trait and the risk of Plasmodium falciparum malaria and ... transfusion in sicklecelldisease study group Blood 1997, 89:1533-1542 13 Ritterbach C, Burkle H, Durken M, Wappler F: Anesthesiological management in patients with sicklecelldisease Anesthesiol...
... Accepted: June 2010 Published: June 2010 References Serjeant G, Serjeant B: Nomenclature and genetics of SickleCellDiseaseSickleCellDisease Oxford: Oxford University PressSerjeant G, Serjeant ... in sicklecelldiseaseJ Natl Med Assoc 2003, 95:533-537 Molock SD, Belgrave FZ: Depression and anxiety in patients with sicklecell disease: conceptual and methodological considerations J Health ... Orringer E, Strayhorn D: Depression, disease severity, andsicklecelldiseaseJ Behav Med 1999, 22:115-126 Jenerette C, Funk M, Murdaugh C: Sicklecell disease: a stigmatizing condition that...
... MH, Klug PP: Mortality in sicklecell disease: life expectancy and risk factors for early death N Engl J Med 1994, 330:1639-44 Powars D, Weidman JA, Odom-Maryon T, Niland JC, Johnson C: Sicklecell ... of 48 children with asthma andsicklecelldiseaseand compared them to a control group of 48 children with sicklecelldisease alone The 48 children with sicklecelland asthma represented all ... children with both asthma andsicklecelldisease are significantly more likely to develop severe complications of sicklecelldisease including acute chest syndrome and cerebral vascular accidents...
... between knowledge about the cause(s) of sicklecelldisease of the participants and their attitude towards their children with sicklecelldisease Knowledge of the impact of sicklecelldisease ... between knowledge about the cause(s) of sicklecelldiseaseand the attitude of parents towards their children with sicklecelldisease Hypothesis 4: Knowledge of the impact of sicklecelldisease ... between knowledge of the participants as par prevention of sicklecelldiseaseand attitude towards their children with sicklecelldisease Table 4: Participants’ knowledge about causes of sickle cell...
... children with sicklecelldisease Journal of Pediatrics, 145, 622-627 Center for Disease Control (2010) SickleCell Disease: Data and Statistics Retrieved from http://www.cdc.gov/ncbddd/sicklecell/data.html ... children with sicklecelldisease Archives of Medical Research, 33, 308-312 Smiley, D., Dagogo-Jack, S., & Umpierrez, G (2008) Therapy insight: Metabolic and endocrine disorders in sicklecelldisease ... B., Kawchak, D A., Zemel, B S., Rovner, A J. , Ohene-Frempong, K. , & Stallings, V A (2008) Markers of bone turnover are associated with growth and development in young subjects with sickle cell...
... Sicklecell disease- S βo DIAGNOSIS AND COUNSELING W ORLD W IDE W EB R ESOURCES SICKLECELLAND GENETIC WEB SITES SickleCellDisease Association of America (SCDAA) http://www.sicklecelldisease.org ... Center for Disease Control and Prevention: Hemoglobin S Allele andSickleCellDisease http://www.cdc.gov/genomics/hugenet/reviews /sickle. htm An excellent article about sicklecell genetics and epidemiology ... Sicklecell disease- SS SCD-SS βs / βc Sicklecell disease- SC SCD-SC βs / / βo thalassemia βs / β+ thalassemia thalassemia SCD-S βo thal Sicklecell disease- S β+ thalassemia SCD-S β+ thal Sickle...
... Introduction SickleCellDiseaseSicklecelldisease is a genetic disorder that decreases life expectancy by 25 to 30 years and affects approximately 80,000 Americans.1,2 Sicklecelldisease refers ... short and long-term harms of its use in patients with sicklecelldiseaseand other diseases, and to discuss barriers to the use of hydroxyurea and other medications in the treatment of sicklecell ... from Randomized Trials in SickleCellDisease 46 Results from Observational Studies in SickleCellDisease Including Case Reports 47 Results from Studies in Other Diseases .50 Key...
... Steinberg MH, Management of SickleCellDisease NEJM 1999 Apr; 340 (13): 1021-30 Fixler J, Styles L SickleCellDisease Pediatr Clin N Am 2002; 49: 1193-1210 Marchant WA, Walker I Anaesthetic Management ... printed physician order Paediatric SickleCellDisease References: Child Health Network: Management of SickleCellDisease in Children Practice Guideline 20042004 Vichinsky EP, Styles LA, Colangelo ... Criteria: Children with sicklecelldiseaseand a fever as defined by an oral temperature of > 38 ºC CPG 21-1 Management of SickleCellDisease in Children Page of 15 Assessment and Treatment: Emergency...
... sicklecelldisease Journal of Pediatric Hematology and Oncolology, 26, 574–578 Porter, L.S., Gil, K. M., Sedway, J. A., Ready, J. , Workman, E & Thompson, R .J (1998) Pain and stress in sicklecell ... with sicklecell disease: a report from the Cooperative Study of SickleCellDisease Journal of Pediatrics, 139, 391–397 Whitten, C.F & Fischoff, J (1974) Psychosocial effects of sicklecelldisease ... Depression in sicklecelldisease Journal of the National Medical Association, 95, 533–537 Hurtig, A.L & Park, K. B (1989) Adjustment and coping in adolescents with sicklecelldisease Annals...
... of children with and without sicklecelldisease In addition, we also compared parents of children with sicklecelldisease to parents of children without sicklecelldiseaseand without other ... with mild sicklecelldiseaseand children without sicklecelldisease In our subset analysis (Figure 1) we analyzed the following groups for differences in scores: 1) sicklecelldisease without ... = 47), 2) sicklecelldisease with neurobehavioral co-morbidities (n = 23), 3) sicklecelldisease with medical co-morbidities (n = 12), 4) sicklecelldisease with neurobehavioral and medical...
... JJ, Gil KM, Burchinal M, Kramer KD, Nash KB, Orringer E, Strayhorn D: Depression, disease severity, andsicklecelldiseaseJ Behav Med 1999, 22(2):115-126 Ohaeri JU, Shokunbi WA, Akinlade KS, Dare ... in sicklecelldisease Hematol J 2003, 4(1):71-73 Bodhise PB, Dejoie M, Brandon Z, Simpkins S, Ballas SK: Non-pharmacologic Management of SickleCell Pain Hematology 2004, 9(3):235-237 Strickland ... Depression in sicklecelldiseaseJ Natl Med Assoc 2003, 95(7):533-537 Thomas VJ, Hambleton I, Serjeant G: Psychological distress and coping in sicklecell disease: comparison of British and Jamaican...
... Bone and joint Manifestations of sicklecell anemia J Bone and Joint Surg (Br) 1990, 72B:494-499 10 Badhulkar SS, Pande K, Badhulkur S: The hand-foot syndrome in sicklecell haemoglobinopathy J ... Bone and Joint Surg (Br) 1995, 77B:310-312 11 Acurio MT, Friedman RJ: Hip Arthroplasty in patients with sicklecell Haemoglobinopathy J Bone and Joint Surg (Br) 1992, 71B:367-371 12 Harkess JW: ... 2010, 5:2 http://www.josr-online.com/content/5/1/2 Page of 35 Ware HE, Brooks AP, Toye R, Berney SI: Sicklecelldiseaseand silent avascular necrosis of the hip J Bone and Joint Surg (Br) 1991,...
... 11:645-658 20 Gustafson KE, Bonner MJ, Hardy KK, Thompson RJ: Biopsychosocial and Developmental Isses in SickleCellDisease In Comprehensive Handbook of Childhood Cancer andSickleCellDisease Edited ... and Adolescents with SickleCellDisease In Comprehensive Handbook of Childhood Cancer andSickleCellDisease Edited by: Brown RT Oxford University Press; 2006:471-495 Noll RB, Vannatta K, Koontz ... sicklecell disease: child and parent perception Br J Haematol 2005, 130:437-444 Page of 17 Panepinto JA, Pajewski NM, Foerster LM, Sabnis S, Hoffmann RG: Impact of family income andsickle cell...
... JJ, Gil KM, Burchinal M, Kramer KD, Nash KB, Orringer E, Strayhorn D: Depression, disease severity, andsicklecelldiseaseJ Behav Med 1999, 22(2):115-126 Ohaeri JU, Shokunbi WA, Akinlade KS, Dare ... in sicklecelldisease Hematol J 2003, 4(1):71-73 Bodhise PB, Dejoie M, Brandon Z, Simpkins S, Ballas SK: Non-pharmacologic Management of SickleCell Pain Hematology 2004, 9(3):235-237 Strickland ... Depression in sicklecelldiseaseJ Natl Med Assoc 2003, 95(7):533-537 Thomas VJ, Hambleton I, Serjeant G: Psychological distress and coping in sicklecell disease: comparison of British and Jamaican...
... homozygous sicklecelldisease Eur J Clin Nutr 1989, 43:609-614 63 Houston PE, Rana S, Sekhsaria S, Perlin E, Kim KS, Castro OL: Homocysteine in sicklecell disease: relationship to stroke Am J Med ... pre-albumin and carotenoid levels in sicklecelldisease patients Am J Med Sci 1990, 299:13-15 56 Ndombi IO, Kinoti SN: Serum vitamin E and the sickling status in children with sicklecell anaemia ... in sicklecelldisease Ann NY Acad Sci 2000, 899:375-391 Jain SK, Shohet SB: A novel phospholipid in irreversibly sickled cells: evidence for in vivo peroxidative membrane damage in sickle cell...
... van der Sande JJ, Valk J: Acute Psychosis in a patient with a combination of sicklecelldiseaseand hemoglobin C disease Ned Tijdschr Geneeskd 137(6):302-4 1993 Feb Norman RMG, Malla AK: Stressful ... black race, Arabians and the Caribbean [1] It is a hereditary and chronic medical condition that encompasses sicklecell anemia (SCA) (Hb SS), sicklecell hemoglobin C disease (Hb SC) andsickle ... Mankad V: Depression in children and adolescents with sicklecelldisease Arch Pediatr Adolesc Med 1994, 148(5):457-60 Udofia O, Oseikhuemen AE: Psychiatric morbidity in patients with sickle cell...
... basic kinds of cells: prokaryotic and eukaryotic Prokaryotic cells, including bacteria and archae, although far from simple, are generally much smaller and less complex structurally than eukaryotic ... synthesized on the ER CHAPTER 1: Cells Motility is accomplished by different means in prokaryotic and eukaryotic cells Eukaryotic cells, such as amoebas and white blood cells, creep along substrates ... the cell wall Figure 1-2 A bacterial cell 6 MOLECULAR ANDCELL BIOLOGY These protect the bacteria from predatory cells and promote their attachment to various objects and to each other Most eukaryotic...