-
1
-
-
0034123430
-
Lessons learned from the Stroke Prevention Trial in Sickle Cell Anemia (STOP) study
-
Adams, R.J. (2000). Lessons learned from the Stroke Prevention Trial in Sickle Cell Anemia (STOP) study. Journal of Pediatric Neurology, 15, 344 349.
-
(2000)
Journal of Pediatric Neurology
, vol.15
, pp. 344-349
-
-
Adams, R.J.1
-
2
-
-
2542470807
-
Genetic risk factors for cerebrovascular disease in children with sickle cell disease: Design of a case-control association study and genomewide screen
-
Adams, G.T., Snieder, H., McKie, V.C., Clair, B., Brambilla, D., Adams, R.J., et al. (2003). Genetic risk factors for cerebrovascular disease in children with sickle cell disease: Design of a case-control association study and genomewide screen. BioMed Central Medical Genetics, 4 (1 6.
-
(2003)
BioMed Central Medical Genetics
, vol.4
, Issue.1
, pp. 6
-
-
Adams, G.T.1
Snieder, H.2
McKie, V.C.3
Clair, B.4
Brambilla, D.5
Adams, R.J.6
-
3
-
-
0036181101
-
Health supervision for children with sickle cell disease
-
American Academy of Pediatrics (AAP), Section on Hematology/Oncology, Committee on Genetics
-
American Academy of Pediatrics (AAP), Section on Hematology/Oncology, Committee on Genetics 2002). Health supervision for children with sickle cell disease. Pediatrics, 109 (3 526 535.
-
(2002)
Pediatrics
, vol.109
, Issue.3
, pp. 526-535
-
-
-
4
-
-
0034178262
-
Sickle hemoglobin (HbS) allele and sickle cell disease: A HuGE review
-
&
-
Ashley-Koch, A., Yang, Q., & Olney, R.S. (2000). Sickle hemoglobin (HbS) allele and sickle cell disease: A HuGE review. American Journal of Epidemiology, 151 (9 839 845.
-
(2000)
American Journal of Epidemiology
, vol.151
, Issue.9
, pp. 839-845
-
-
Ashley-Koch, A.1
Yang, Q.2
Olney, R.S.3
-
5
-
-
0035525732
-
Discrepancies between genotype and phenotype in hematology: An important frontier
-
Beutler, E. (2001). Discrepancies between genotype and phenotype in hematology: An important frontier. Blood, 98 (9 2597 2602.
-
(2001)
Blood
, vol.98
, Issue.9
, pp. 2597-2602
-
-
Beutler, E.1
-
6
-
-
33745504900
-
-
Boys Town National Research Hospital. n.d.). Retrieved August 16, 2005, from
-
Boys Town National Research Hospital n.d.). The national center for the study and treatment of Usher syndrome. Retrieved August 16, 2005, from http://www.boystownhospital.org/usher/index.asp
-
The National Center for the Study and Treatment of Usher Syndrome
-
-
-
7
-
-
33745492893
-
The urgent need for early detection of deafness in infants
-
Brown, E.W. (1998). The urgent need for early detection of deafness in infants. Medical Update, 22, 2.
-
(1998)
Medical Update
, vol.22
, pp. 2
-
-
Brown, E.W.1
-
8
-
-
12944287077
-
Sickle cell disease
-
&
-
Buchanan, G.R., DeBaun, M.R., Quinn, C.T., & Steinberg, M.H. (2004). Sickle cell disease. Hematology, 1, 35.
-
(2004)
Hematology
, vol.1
, pp. 35
-
-
Buchanan, G.R.1
Debaun, M.R.2
Quinn, C.T.3
Steinberg, M.H.4
-
9
-
-
0035139122
-
Sickle cell disease: No longer a single gene disorder
-
&
-
Chui, D., & Dover, G. (2001). Sickle cell disease: No longer a single gene disorder. Current Opinion Pediatrics, 13, 23 37.
-
(2001)
Current Opinion Pediatrics
, vol.13
, pp. 23-37
-
-
Chui, D.1
Dover, G.2
-
10
-
-
33745504157
-
-
Early diagnosis of Usher syndrome type 1 made possible by new findings. Retrieved May 20, 2005, from
-
Early diagnosis of Usher syndrome type 1 made possible by new findings 2003). Retrieved May 20, 2005, from http://www.nicd.nih.gov/news/releases/03/ 04_23_03.asp
-
(2003)
-
-
-
11
-
-
22144454637
-
Nursing leadership in genomics for health and society
-
&
-
Feetham, S., Thomson, E.J., & Hinshaw, A.S. (2005). Nursing leadership in genomics for health and society. Journal of Nursing Scholarship, 37, 102 110.
-
(2005)
Journal of Nursing Scholarship
, vol.37
, pp. 102-110
-
-
Feetham, S.1
Thomson, E.J.2
Hinshaw, A.S.3
-
12
-
-
3142590376
-
Declining stroke rates in children with sickle cell disease
-
&
-
Fullerton, H.J., Adams, R.J., Zhao, S., & Johnston, S. (2004). Declining stroke rates in children with sickle cell disease. Blood, 104, 336 339.
-
(2004)
Blood
, vol.104
, pp. 336-339
-
-
Fullerton, H.J.1
Adams, R.J.2
Zhao, S.3
Johnston, S.4
-
13
-
-
0035693480
-
Cystic fibrosis carrier screening: Steps in the development of a mutation panel
-
Gilbert, F. (2001). Cystic fibrosis carrier screening: Steps in the development of a mutation panel. Genetic Testing, 5 (3 223 227.
-
(2001)
Genetic Testing
, vol.5
, Issue.3
, pp. 223-227
-
-
Gilbert, F.1
-
14
-
-
0038107362
-
Distinct HLA associations by stroke subtype in children with sickle cell anemia
-
&
-
Hoppe, C., Klitz, W., Vigil, L., Vichinsky, E., & Styles, L. (2003). Distinct HLA associations by stroke subtype in children with sickle cell anemia. Blood, 101 (7 2865 2869.
-
(2003)
Blood
, vol.101
, Issue.7
, pp. 2865-2869
-
-
Hoppe, C.1
Klitz, W.2
Vigil, L.3
Vichinsky, E.4
Styles, L.5
-
15
-
-
1542283710
-
Gene interactions and stroke risk in children with sickle cell anemia
-
Hoppe, C., Klitz, W., Cheng, S., Apple, R., Steiner, L., Robles, L., et al. (2004). Gene interactions and stroke risk in children with sickle cell anemia. Blood, 103 (6 2391 2396.
-
(2004)
Blood
, vol.103
, Issue.6
, pp. 2391-2396
-
-
Hoppe, C.1
Klitz, W.2
Cheng, S.3
Apple, R.4
Steiner, L.5
Robles, L.6
-
16
-
-
0036591556
-
Simple fluorescent PCR assay for discriminating FRAXA fully mutated females from normal homozygotes
-
Houdayer, C., Lourdaux, J., Billette de Villemeur, T., Royer-Legrain, G., Bahuau, M., Bonnefont, J.P., et al. (2002). Simple fluorescent PCR assay for discriminating FRAXA fully mutated females from normal homozygotes. Genetic Testing, 6 (2 135 139.
-
(2002)
Genetic Testing
, vol.6
, Issue.2
, pp. 135-139
-
-
Houdayer, C.1
Lourdaux, J.2
Billette De Villemeur, T.3
Royer-Legrain, G.4
Bahuau, M.5
Bonnefont, J.P.6
-
17
-
-
33745499566
-
-
& Retrieved May 20, 2005, from
-
Kimberling, W.J., Weston, M.D., & Orten, D.J. (2004). Usher syndrome type II. Retrieved May 20, 2005, from http://www.genetests.org
-
(2004)
Usher Syndrome Type II
-
-
Kimberling, W.J.1
Weston, M.D.2
Orten, D.J.3
-
18
-
-
33745499566
-
-
& Retrieved May 20, 2005, from
-
Kimberling, W.J., Weston, M.D., & Pieke-Dahl, S.P. (2004, February 6). Usher syndrome type I. Retrieved May 20, 2005, from http://www.genetests.org
-
(2004)
Usher Syndrome Type I
-
-
Kimberling, W.J.1
Weston, M.D.2
Pieke-Dahl, S.P.3
-
19
-
-
0344676391
-
Is there a genetic basis for pediatric stroke?
-
Kirkham, F. (2003). Is there a genetic basis for pediatric stroke? Current Opinion in Pediatrics, 15 (6 547 558.
-
(2003)
Current Opinion in Pediatrics
, vol.15
, Issue.6
, pp. 547-558
-
-
Kirkham, F.1
-
20
-
-
0036964933
-
Newborn screening: New opportunities and new challenges
-
Lashley, F.R. (2002). Newborn screening: New opportunities and new challenges. Newborn and Infant Nursing Reviews, 2 (4 228 242.
-
(2002)
Newborn and Infant Nursing Reviews
, vol.2
, Issue.4
, pp. 228-242
-
-
Lashley, F.R.1
-
21
-
-
0041528191
-
Lessons from the past? Looking to the future. Newborn screening
-
Levy, H.L. (2003). Lessons from the past? Looking to the future. Newborn screening. Pediatric Annals, 32 (8 505 508.
-
(2003)
Pediatric Annals
, vol.32
, Issue.8
, pp. 505-508
-
-
Levy, H.L.1
-
22
-
-
9644270359
-
A novel sickle hemoglobin: Hemoglobin S-South End
-
Luo, H., Adewoye, A.H., Eung, S., Skelton, T.P., Quillen, K., McMahon, L., et al. (2004). A novel sickle hemoglobin: Hemoglobin S-South End. Journal of Pediatric Hematology/Oncology, 26 (11 773 776.
-
(2004)
Journal of Pediatric Hematology/Oncology
, vol.26
, Issue.11
, pp. 773-776
-
-
Luo, H.1
Adewoye, A.H.2
Eung, S.3
Skelton, T.P.4
Quillen, K.5
McMahon, L.6
-
23
-
-
0242706345
-
Births: Final data for 2002
-
&
-
Martin, J.A., Hamilton, B.E., Sutton, P.D., Ventura, S.J., Menacker, F., & Munson, M.L. (2003). Births: Final data for 2002. National Vital Statistics Report, 52 (10 1 114.
-
(2003)
National Vital Statistics Report
, vol.52
, Issue.10
, pp. 1-114
-
-
Martin, J.A.1
Hamilton, B.E.2
Sutton, P.D.3
Ventura, S.J.4
Menacker, F.5
Munson, M.L.6
-
24
-
-
16844386404
-
Defining stroke risk in sickle cell anemia
-
&
-
Meschia, J.G., & Pankratz, V.S. (2005). Defining stroke risk in sickle cell anemia. Nature Genetics, 37, 340 341.
-
(2005)
Nature Genetics
, vol.37
, pp. 340-341
-
-
Meschia, J.G.1
Pankratz, V.S.2
-
25
-
-
0026076686
-
Sickle cell disease as a cause of osteonecrosis of the femoral head
-
&
-
Milner, P.F., Kraus, A.P., Sebes, J.I., Sleeper, L.A., Dukes, K.A., & Embury, S.H. (1991). Sickle cell disease as a cause of osteonecrosis of the femoral head. New England Journal of Medicine, 325, 1476 1481.
-
(1991)
New England Journal of Medicine
, vol.325
, pp. 1476-1481
-
-
Milner, P.F.1
Kraus, A.P.2
Sebes, J.I.3
Sleeper, L.A.4
Dukes, K.A.5
Embury, S.H.6
-
26
-
-
21344458142
-
From genetics to genomics: Using gene-based medicine to prevent and promote health in children
-
&
-
Moore, C.A., Khoury, M.J., & Bradley, L.A. (2005, June). From genetics to genomics: Using gene-based medicine to prevent and promote health in children. Seminars in Perinatology, 29 (3 135 143.
-
(2005)
Seminars in Perinatology
, vol.29
, Issue.3
, pp. 135-143
-
-
Moore, C.A.1
Khoury, M.J.2
Bradley, L.A.3
-
27
-
-
0023929164
-
Sickle cell-hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromes
-
&
-
Murray, N., Serjeant, B.E., & Serjeant, G.R. (1988). Sickle cell-hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromes. British Journal of Haematology, 69, 89 92.
-
(1988)
British Journal of Haematology
, vol.69
, pp. 89-92
-
-
Murray, N.1
Serjeant, B.E.2
Serjeant, G.R.3
-
28
-
-
16844378581
-
Listening to genetic background noise
-
Nadeau, J.H. (2005). Listening to genetic background noise. New England Journal of Medicine, 352 (15 1598 1599.
-
(2005)
New England Journal of Medicine
, vol.352
, Issue.15
, pp. 1598-1599
-
-
Nadeau, J.H.1
-
29
-
-
9244253915
-
-
National Coalition of Health Professional Education in Genetics. Retrieved June 20, 2004, from http://www.nchpeg.org/eduresources/core/core.asp
-
National Coalition of Health Professional Education in Genetics 2004). Core competencies in genetics essential for all health-care professionals. Retrieved June 20, 2004, from http://www.nchpeg.org/nchpeg.html? http://www.nchpeg.org/eduresources/core/core.asp
-
(2004)
Core Competencies in Genetics Essential for All Health-care Professionals
-
-
-
31
-
-
0031965089
-
Cerebrovascular accidents in sickle cell disease: Rates and risk factors
-
Ohene-Frempong, K., Weiner, S.J., Sleeper, L.A., Miller, S.T., Embury, S., Moohr, J.W., et al. (1998). Cerebrovascular accidents in sickle cell disease: Rates and risk factors. Blood, 91, 288 294.
-
(1998)
Blood
, vol.91
, pp. 288-294
-
-
Ohene-Frempong, K.1
Weiner, S.J.2
Sleeper, L.A.3
Miller, S.T.4
Embury, S.5
Moohr, J.W.6
-
32
-
-
7044235524
-
Risk factors and prediction of outcomes in children and adolescents who have sickle cell anemia
-
&
-
Quinn, C.T., & Miller, S.T. (2004). Risk factors and prediction of outcomes in children and adolescents who have sickle cell anemia. Hematology/oncology Clinics of North America, 18 (6 1339 1354.
-
(2004)
Hematology/oncology Clinics of North America
, vol.18
, Issue.6
, pp. 1339-1354
-
-
Quinn, C.T.1
Miller, S.T.2
-
33
-
-
2542455639
-
Survival of children with sickle cell disease
-
&
-
Quinn, C.T., Rogers, Z.R., & Buchanan, G.R. (2004). Survival of children with sickle cell disease. Blood, 103 (11 4023 4027.
-
(2004)
Blood
, vol.103
, Issue.11
, pp. 4023-4027
-
-
Quinn, C.T.1
Rogers, Z.R.2
Buchanan, G.R.3
-
34
-
-
8744243196
-
Interactions of biomedical and environmental risk factors for cognitive development: A preliminary study of sickle cell disease
-
&
-
Schatz, J., Finke, R.B.S., & Roberts, C.W. (2004). Interactions of biomedical and environmental risk factors for cognitive development: A preliminary study of sickle cell disease. Journal of Developmental & Behavioral Pediatrics, 25 (5 303 310.
-
(2004)
Journal of Developmental & Behavioral Pediatrics
, vol.25
, Issue.5
, pp. 303-310
-
-
Schatz, J.1
Finke, R.B.S.2
Roberts, C.W.3
-
35
-
-
16844366938
-
Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia
-
&
-
Sebastiani, P., Ramoni, M.F., Nolan, V., Baldwin, C.T., & Steinberg, M.H. (2005). Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia. Nature Genetics, 37, 435 444.
-
(2005)
Nature Genetics
, vol.37
, pp. 435-444
-
-
Sebastiani, P.1
Ramoni, M.F.2
Nolan, V.3
Baldwin, C.T.4
Steinberg, M.H.5
-
36
-
-
33745496748
-
-
& Retrieved May 29, 2004, from
-
Smith, R.J., Green, G.E., & Van Camp, G. (2003). Deafness and hereditary hearing loss. Retrieved May 29, 2004, from http://www.geneclinics. org/profiles/deafness-overview/details.html
-
(2003)
Deafness and Hereditary Hearing Loss
-
-
Smith, R.J.1
Green, G.E.2
Van Camp, G.3
-
37
-
-
0021254222
-
Effects of thalassemia and microcytosis on the hematologic and vasooclusive severity of sickle cell anemia
-
&
-
Steinberg, M.H., Rosenstock, W., Coleman, M.B., Adams, J.G., Platica, O., & Cedeno, M. (1984). Effects of thalassemia and microcytosis on the hematologic and vasooclusive severity of sickle cell anemia. Blood, 63, 1353 1360.
-
(1984)
Blood
, vol.63
, pp. 1353-1360
-
-
Steinberg, M.H.1
Rosenstock, W.2
Coleman, M.B.3
Adams, J.G.4
Platica, O.5
Cedeno, M.6
-
38
-
-
0001719775
-
Compound heterozygous and other sickle hemoglobinopathies
-
In. M.J. Steinberg, B.G. Forget, D.R. Higgs, & R.L. Nagel (. Eds. pp.). Cambridge, MA: Cambridge University Press.
-
Steinberg, M.H. (2001). Compound heterozygous and other sickle hemoglobinopathies. In M.J. Steinberg, B.G. Forget, D.R. Higgs, & R.L. Nagel (Eds. Disorders of hemoglobin genetics, pathophysiology, and clinical management (pp. 786 810). Cambridge, MA : Cambridge University Press.
-
(2001)
Disorders of Hemoglobin Genetics, Pathophysiology, and Clinical Management
, pp. 786-810
-
-
Steinberg, M.H.1
-
39
-
-
0038654384
-
Pathophysiological-based approaches to treatment of sickle cell disease
-
&
-
Steinberg, M.H., & Brugnara, C. (2003). Pathophysiological-based approaches to treatment of sickle cell disease. Annual Review of Medicine, 54, 89 112.
-
(2003)
Annual Review of Medicine
, vol.54
, pp. 89-112
-
-
Steinberg, M.H.1
Brugnara, C.2
-
40
-
-
0034210945
-
Evidence for HLA-related susceptibility for stroke in children with sickle cell disease
-
&
-
Styles, L.A., Hoppe, C., Klitz, W., Vichinsky, E., Lubin, B., & Trachtenberg, E. (2000). Evidence for HLA-related susceptibility for stroke in children with sickle cell disease. Blood, 95, 3562 3567.
-
(2000)
Blood
, vol.95
, pp. 3562-3567
-
-
Styles, L.A.1
Hoppe, C.2
Klitz, W.3
Vichinsky, E.4
Lubin, B.5
Trachtenberg, E.6
-
41
-
-
0037114628
-
Variant in the VCAM1 gene and risk of symptomatic stroke in sickle cell disease
-
Taylor, J.G.T., Tang, D.C., Savage, S.A., Leitman, S.F., Heller, S.I., Sergeant, G.R., et al. (2002). Variant in the VCAM1 gene and risk of symptomatic stroke in sickle cell disease. Blood, 100, 4303 4309.
-
(2002)
Blood
, vol.100
, pp. 4303-4309
-
-
Taylor, J.G.T.1
Tang, D.C.2
Savage, S.A.3
Leitman, S.F.4
Heller, S.I.5
Sergeant, G.R.6
-
42
-
-
0030890407
-
Benign clinical course in homozygous sickle cell disease: A search for predictors
-
&
-
Thomas, P.W., Higgs, D.R., & Serjeant, G.R. (1997). Benign clinical course in homozygous sickle cell disease: A search for predictors. Journal of Clinical Epidemiology, 50, 121 126.
-
(1997)
Journal of Clinical Epidemiology
, vol.50
, pp. 121-126
-
-
Thomas, P.W.1
Higgs, D.R.2
Serjeant, G.R.3
-
43
-
-
33745481075
-
-
Usher Syndrome. Retrieved May 20, 2005, from
-
Usher Syndrome 2003, February 23). Retrieved May 20, 2005, from http://www.nidcd.nih.gov/health/hearing/usher.asp
-
(2003)
-
-
-
44
-
-
33745486702
-
-
Usher Syndrome Type II. Retrieved May 20, 2005, from
-
Usher Syndrome Type II 2005, May 13). Retrieved May 20, 2005, from http://ghr.nlm.nih.gov/condition=ushersyndrometypeii
-
(2005)
-
-
-
45
-
-
33745511378
-
-
Usher Syndrome Type III. Retrieved May 20, 2005 from
-
Usher Syndrome Type III 2005). Retrieved May 20, 2005 from http:/ghr.nlm.nih.gov/condition=ushersyndrometypeiii.
-
(2005)
-
-
-
46
-
-
84876571521
-
-
& Gene reviews. Retrieved December 31, 2004, from
-
Vichinsky, E., & Schlis, K. (2003). Sickle cell disease. Gene reviews. Retrieved December 31, 2004, from http://www.geneclinics.org/servlet/ access?id=8888891&key=G1Jpe7vE9z8Ch&gry=INSERTGRY&fcn=y&fw= th91&filename=/profiles/sickle/index.html
-
(2003)
Sickle Cell Disease
-
-
Vichinsky, E.1
Schlis, K.2
-
47
-
-
0242407562
-
Pharmacological treatment of monogenic disease
-
Weatherall, D.J. (2003). Pharmacological treatment of monogenic disease. The Pharmacogenomics Journal, 3 (5 264 266.
-
(2003)
The Pharmacogenomics Journal
, vol.3
, Issue.5
, pp. 264-266
-
-
Weatherall, D.J.1
|