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Comparison of treatment outcomes of childhood Hodgkin lymphoma in two US centers and a center in Recife, Brazil. [electronic resource] by
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- Hudson, Melissa M
- Pedrosa, Francisco
- Lins, Mecneide
- Pedrosa, Marcia
- Barros, Cynthia
- Maciel, Kaline
- Pui, Ching-Hon
- Ribeiro, Raul C
- Howard, Scott C
Producer: 20070824
In:
Pediatric blood & cancer vol. 49
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Thermodynamic criterion for the conformation of P1 residues of substrates and of inhibitors in complexes with serine proteinases. [electronic resource] by
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- James, M N
- Anderson, S
- Song, J
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- Saunders, C W
- Laskowski, M
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In:
Biochemistry vol. 38
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A comparison of surgical and radiotherapy breast cancer therapy utilization in Canada (British Columbia), Scotland (Dundee), and Australia (Western Australia) with models of "optimal" therapy. [electronic resource] by
- Fong, A
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- Olivotto, I A
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- Jacob, S
- Ng, W
- Speers, C
- Delaney, G P
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In:
Breast (Edinburgh, Scotland) vol. 21
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Handling of radioactive seed localisation breast specimens in the histopathology laboratory: the Western Australian experience. [electronic resource] by
- Dessauvagie, B F
- Frost, F A
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- Hardie, M
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- Burrage, J
- Bourke, A
- Taylor, D
- Kamyab, R
- Saunders, C
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In:
Pathology vol. 47
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Lung clearance index is a sensitive, repeatable and practical measure of airways disease in adults with cystic fibrosis. [electronic resource] by
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- Gustafsson, P M
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- Saunders, C
- Greening, A P
- Porteous, D J
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- Alton, E W F W
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In:
Thorax vol. 63
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The utility of computerized neuropsychological assessment of cognitive dysfunction in patients with relapsing-remitting multiple sclerosis. [electronic resource] by
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- Usiskin, J B
- Quig, M E
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- Saunders, C
- Crayton, H
- Mandler, R
- Kerr, D
- Reeves, D
- Fuchs, K
- Manning, C
- Keller, M
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In:
Multiple sclerosis (Houndmills, Basingstoke, England) vol. 9
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When knowledge of a heritable gene mutation comes out of the blue: treatment-focused genetic testing in women newly diagnosed with breast cancer. [electronic resource] by
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- Quinn, V F
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- Kirk, J
- Tucker, K M
- Rahman, B
- Saunders, C
- Watts, K J
- Peate, M
- Geelhoed, E
- Barlow-Stewart, K
- Field, M
- Harris, M
- Antill, Y C
- Mitchell, G
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In:
European journal of human genetics : EJHG vol. 24
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The association between different night shiftwork factors and breast cancer: a case-control study. [electronic resource] by
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- Erren, T C
- Glass, D C
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- Saunders, C
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- El-Zaemey, S
- Rogers, P
- Peters, S
- Slevin, T
- D'Orsogna, A
- de Vocht, F
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- Heyworth, J S
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In:
British journal of cancer vol. 109
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330.
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SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking. [electronic resource] by
- Bowton, E
- Saunders, C
- Reddy, I A
- Campbell, N G
- Hamilton, P J
- Henry, L K
- Coon, H
- Sakrikar, D
- Veenstra-VanderWeele, J M
- Blakely, R D
- Sutcliffe, J
- Matthies, H J G
- Erreger, K
- Galli, A
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In:
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Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings. [electronic resource] by
- Caylor, R C
- Grote, L
- Thiffault, I
- Farrow, E G
- Willig, L
- Soden, S
- Amudhavalli, S M
- Nopper, A J
- Horii, K A
- Fleming, E
- Jenkins, J
- Welsh, H
- Ilyas, M
- Engleman, K
- Abdelmoity, A
- Saunders, C J
Producer: 20190926
In:
Neurogenetics vol. 19
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332.
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Correction to: Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings. [electronic resource] by
- Caylor, R C
- Grote, L
- Thiffault, I
- Farrow, E G
- Willig, L
- Soden, S
- Amudhavalli, S M
- Nopper, A J
- Horii, K A
- Fleming, E
- Jenkins, J
- Welsh, H
- Ilyas, M
- Engleman, K
- Abdelmoity, A
- Saunders, C J
Publication details: Neurogenetics 12 2018
In:
Neurogenetics vol. 19
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Drosophila melanogaster: a novel animal model for the behavioral characterization of autism-associated mutations in the dopamine transporter gene. [electronic resource] by
- Hamilton, P J
- Campbell, N G
- Sharma, S
- Erreger, K
- Hansen, F H
- Saunders, C
- Belovich, A N
- Sahai, M A
- Cook, E H
- Gether, U
- McHaourab, H S
- Matthies, H J G
- Sutcliffe, J S
- Galli, A
Producer: 20140623
In:
Molecular psychiatry vol. 18
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De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder. [electronic resource] by
- Hamilton, P J
- Campbell, N G
- Sharma, S
- Erreger, K
- Herborg Hansen, F
- Saunders, C
- Belovich, A N
- Sahai, M A
- Cook, E H
- Gether, U
- McHaourab, H S
- Matthies, H J G
- Sutcliffe, J S
- Galli, A
Producer: 20140623
In:
Molecular psychiatry vol. 18
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Systematic review of the impact of breast-conserving surgery on cancer outcomes of multiple ipsilateral breast cancers. [electronic resource] by
- Winters, Z E
- Horsnell, J
- Elvers, K T
- Maxwell, A J
- Jones, L J
- Shaaban, A M
- Schmid, P
- Williams, N R
- Beswick, A
- Greenwood, R
- Ingram, J C
- Saunders, C
- Vaidya, J S
- Esserman, L
- Jatoi, I
- Brunt, A M
Publication details: BJS open Aug 2018
In:
BJS open vol. 2
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Observation versus late reintroduction of letrozole as adjuvant endocrine therapy for hormone receptor-positive breast cancer (ANZ0501 LATER): an open-label randomised, controlled trial. [electronic resource] by
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- Forbes, J F
- Boyle, F M
- Kannourakis, G
- Gill, P G
- Bayliss, E
- Saunders, C
- Della-Fiorentina, S
- Kling, N
- Campbell, I
- Mann, G B
- Coates, A S
- Gebski, V
- Davies, L
- Thornton, R
- Reaby, L
- Cuzick, J
- Green, M
Producer: 20171221
In:
Annals of oncology : official journal of the European Society for Medical Oncology vol. 27
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Liver transplantation for "very early" intrahepatic cholangiocarcinoma: International retrospective study supporting a prospective assessment. [electronic resource] by
- Sapisochin, G
- Facciuto, M
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- Marti, J
- Mehta, N
- Yao, F Y
- Vibert, E
- Cherqui, D
- Grant, D R
- Hernandez-Alejandro, R
- Dale, C H
- Cucchetti, A
- Pinna, A
- Hwang, S
- Lee, S G
- Agopian, V G
- Busuttil, R W
- Rizvi, S
- Heimbach, J K
- Montenovo, M
- Reyes, J
- Cesaretti, M
- Soubrane, O
- Reichman, T
- Seal, J
- Kim, P T W
- Klintmalm, G
- Sposito, C
- Mazzaferro, V
- Dutkowski, P
- Clavien, P A
- Toso, C
- Majno, P
- Kneteman, N
- Saunders, C
- Bruix, J
Producer: 20170731
In:
Hepatology (Baltimore, Md.) vol. 64
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MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement. [electronic resource] by
- Donkervoort, S
- Sabouny, R
- Yun, P
- Gauquelin, L
- Chao, K R
- Hu, Y
- Al Khatib, I
- Töpf, A
- Mohassel, P
- Cummings, B B
- Kaur, R
- Saade, D
- Moore, S A
- Waddell, L B
- Farrar, M A
- Goodrich, J K
- Uapinyoying, P
- Chan, S H S
- Javed, A
- Leach, M E
- Karachunski, P
- Dalton, J
- Medne, L
- Harper, A
- Thompson, C
- Thiffault, I
- Specht, S
- Lamont, R E
- Saunders, C
- Racher, H
- Bernier, F P
- Mowat, D
- Witting, N
- Vissing, J
- Hanson, R
- Coffman, K A
- Hainlen, M
- Parboosingh, J S
- Carnevale, A
- Yoon, G
- Schnur, R E
- Boycott, K M
- Mah, J K
- Straub, V
- Foley, A Reghan
- Innes, A M
- Bönnemann, C G
- Shutt, T E
Producer: 20200903
In:
Acta neuropathologica vol. 138
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