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An Adverse Family Environment During Adolescence Predicts Marijuana Use and Antisocial Personality Disorder in Adulthood.

Journal of child and family studies

Lee JY, Brook JS, Finch SJ, Brook DW.
PMID: 27034610
J Child Fam Stud. 2016 Feb;25(2):661-668. doi: 10.1007/s10826-015-0246-z. Epub 2015 Jul 17.

Adult maladaptive behaviors including antisocial personality disorder (ASPD) and marijuana use are major public health concerns. At the present time, there is a dearth of research showing the interrelationships among the possible predictors of adult maladaptive behaviors (i.e., ASPD...

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Lee JY, Brook JS, Finch SJ, et al. An Adverse Family Environment During Adolescence Predicts Marijuana Use and Antisocial Personality Disorder in Adulthood. J Child Fam Stud. 2015;25(2):661-668doi: 10.1007/s10826-015-0246-z.
Lee, J. Y., Brook, J. S., Finch, S. J., & Brook, D. W. (2016). An Adverse Family Environment During Adolescence Predicts Marijuana Use and Antisocial Personality Disorder in Adulthood. Journal of child and family studies, 25(2), 661-668. https://doi.org/10.1007/s10826-015-0246-z
Lee, Jung Yeon, et al. "An Adverse Family Environment During Adolescence Predicts Marijuana Use and Antisocial Personality Disorder in Adulthood." Journal of child and family studies vol. 25,2 (2016): 661-668. doi: https://doi.org/10.1007/s10826-015-0246-z
Lee JY, Brook JS, Finch SJ, Brook DW. An Adverse Family Environment During Adolescence Predicts Marijuana Use and Antisocial Personality Disorder in Adulthood. J Child Fam Stud. 2016 Feb;25(2):661-668. doi: 10.1007/s10826-015-0246-z. Epub 2015 Jul 17. PMID: 27034610; PMCID: PMC4809674.
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Carbon isotopes characterize rapid changes in atmospheric carbon dioxide during the last deglaciation.

Proceedings of the National Academy of Sciences of the United States of America

Bauska TK, Baggenstos D, Brook EJ, Mix AC, Marcott SA, Petrenko VV, Schaefer H, Severinghaus JP, Lee JE.
PMID: 26976561
Proc Natl Acad Sci U S A. 2016 Mar 29;113(13):3465-70. doi: 10.1073/pnas.1513868113. Epub 2016 Mar 14.

An understanding of the mechanisms that control CO2 change during glacial-interglacial cycles remains elusive. Here we help to constrain changing sources with a high-precision, high-resolution deglacial record of the stable isotopic composition of carbon in CO2(δ(13)C-CO2) in air extracted...

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Bauska TK, Baggenstos D, Brook EJ, et al. Carbon isotopes characterize rapid changes in atmospheric carbon dioxide during the last deglaciation. Proc Natl Acad Sci U S A. 2016;113(13):3465-70doi: 10.1073/pnas.1513868113.
Bauska, T. K., Baggenstos, D., Brook, E. J., Mix, A. C., Marcott, S. A., Petrenko, V. V., Schaefer, H., Severinghaus, J. P., & Lee, J. E. (2016). Carbon isotopes characterize rapid changes in atmospheric carbon dioxide during the last deglaciation. Proceedings of the National Academy of Sciences of the United States of America, 113(13), 3465-70. https://doi.org/10.1073/pnas.1513868113
Bauska, Thomas K, et al. "Carbon isotopes characterize rapid changes in atmospheric carbon dioxide during the last deglaciation." Proceedings of the National Academy of Sciences of the United States of America vol. 113,13 (2016): 3465-70. doi: https://doi.org/10.1073/pnas.1513868113
Bauska TK, Baggenstos D, Brook EJ, Mix AC, Marcott SA, Petrenko VV, Schaefer H, Severinghaus JP, Lee JE. Carbon isotopes characterize rapid changes in atmospheric carbon dioxide during the last deglaciation. Proc Natl Acad Sci U S A. 2016 Mar 29;113(13):3465-70. doi: 10.1073/pnas.1513868113. Epub 2016 Mar 14. PMID: 26976561; PMCID: PMC4822573.
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Non-blood circulating tumor DNA detection in cancer.

Oncotarget

Peng M, Chen C, Hulbert A, Brock MV, Yu F.
PMID: 28978187
Oncotarget. 2017 Aug 04;8(40):69162-69173. doi: 10.18632/oncotarget.19942. eCollection 2017 Sep 15.

Tumor DNA contains specific somatic alterations that are crucial for the diagnosis and treatment of cancer. Due to the spatial and temporal intra-tumor heterogeneity, multi-sampling is needed to adequately characterize the somatic alterations. Tissue biopsy, however, is limited by...

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Peng M, Chen C, Hulbert A, et al. Non-blood circulating tumor DNA detection in cancer. Oncotarget. 2017;8(40):69162-69173doi: 10.18632/oncotarget.19942.
Peng, M., Chen, C., Hulbert, A., Brock, M. V., & Yu, F. (2017). Non-blood circulating tumor DNA detection in cancer. Oncotarget, 8(40), 69162-69173. https://doi.org/10.18632/oncotarget.19942
Peng, Muyun, et al. "Non-blood circulating tumor DNA detection in cancer." Oncotarget vol. 8,40 (2017): 69162-69173. doi: https://doi.org/10.18632/oncotarget.19942
Peng M, Chen C, Hulbert A, Brock MV, Yu F. Non-blood circulating tumor DNA detection in cancer. Oncotarget. 2017 Aug 04;8(40):69162-69173. doi: 10.18632/oncotarget.19942. eCollection 2017 Sep 15. PMID: 28978187; PMCID: PMC5620327.
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Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association Consortium.

The journal of pathology. Clinical research

Howat WJ, Blows FM, Provenzano E, Brook MN, Morris L, Gazinska P, Johnson N, McDuffus LA, Miller J, Sawyer EJ, Pinder S, van Deurzen CH, Jones L, Sironen R, Visscher D, Caldas C, Daley F, Coulson P, Broeks A, Sanders J, Wesseling J, Nevanlinna H, Fagerholm R, Blomqvist C, Heikkilä P, Ali HR, Dawson SJ, Figueroa J, Lissowska J, Brinton L, Mannermaa A, Kataja V, Kosma VM, Cox A, Brock IW, Cross SS, Reed MW, Couch FJ, Olson JE, Devillee P, Mesker WE, Seyaneve CM, Hollestelle A, Benitez J, Perez JI, Menéndez P, Bolla MK, Easton DF, Schmidt MK, Pharoah PD, Sherman ME, García-Closas M.
PMID: 27499890
J Pathol Clin Res. 2014 Dec 04;1(1):18-32. doi: 10.1002/cjp2.3. eCollection 2015 Jan.

Breast cancer risk factors and clinical outcomes vary by tumour marker expression. However, individual studies often lack the power required to assess these relationships, and large-scale analyses are limited by the need for high throughput, standardized scoring methods. To...

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Howat WJ, Blows FM, Provenzano E, et al. Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association Consortium. J Pathol Clin Res. 2014;1(1):18-32doi: 10.1002/cjp2.3.
Howat, W. J., Blows, F. M., Provenzano, E., Brook, M. N., Morris, L., Gazinska, P., Johnson, N., McDuffus, L. A., Miller, J., Sawyer, E. J., Pinder, S., van Deurzen, C. H., Jones, L., Sironen, R., Visscher, D., Caldas, C., Daley, F., Coulson, P., Broeks, A., Sanders, J., Wesseling, J., Nevanlinna, H., Fagerholm, R., Blomqvist, C., Heikkilä, P., Ali, H. R., Dawson, S. J., Figueroa, J., Lissowska, J., Brinton, L., Mannermaa, A., Kataja, V., Kosma, V. M., Cox, A., Brock, I. W., Cross, S. S., Reed, M. W., Couch, F. J., Olson, J. E., Devillee, P., Mesker, W. E., Seyaneve, C. M., Hollestelle, A., Benitez, J., Perez, J. I., Menéndez, P., Bolla, M. K., Easton, D. F., Schmidt, M. K., Pharoah, P. D., Sherman, M. E., & García-Closas, M. (2015). Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association Consortium. The journal of pathology. Clinical research, 1(1), 18-32. https://doi.org/10.1002/cjp2.3
Howat, William J, et al. "Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association Consortium." The journal of pathology. Clinical research vol. 1,1 (2015): 18-32. doi: https://doi.org/10.1002/cjp2.3
Howat WJ, Blows FM, Provenzano E, Brook MN, Morris L, Gazinska P, Johnson N, McDuffus LA, Miller J, Sawyer EJ, Pinder S, van Deurzen CH, Jones L, Sironen R, Visscher D, Caldas C, Daley F, Coulson P, Broeks A, Sanders J, Wesseling J, Nevanlinna H, Fagerholm R, Blomqvist C, Heikkilä P, Ali HR, Dawson SJ, Figueroa J, Lissowska J, Brinton L, Mannermaa A, Kataja V, Kosma VM, Cox A, Brock IW, Cross SS, Reed MW, Couch FJ, Olson JE, Devillee P, Mesker WE, Seyaneve CM, Hollestelle A, Benitez J, Perez JI, Menéndez P, Bolla MK, Easton DF, Schmidt MK, Pharoah PD, Sherman ME, García-Closas M. Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association Consortium. J Pathol Clin Res. 2014 Dec 04;1(1):18-32. doi: 10.1002/cjp2.3. eCollection 2015 Jan. PMID: 27499890; PMCID: PMC4858117.
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The different baryonic Tully-Fisher relations at low masses.

Monthly notices of the Royal Astronomical Society

Brook CB, Santos-Santos I, Stinson G.
PMID: 27274704
Mon Not R Astron Soc. 2016 Mar 17;459(1):638-645. doi: 10.1093/mnras/stw650. eCollection 2016 Jun 11.

We compare the Baryonic Tully-Fisher relation (BTFR) of simulations and observations of galaxies ranging from dwarfs to spirals, using various measures of rotational velocity

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Brook CB, Santos-Santos I, Stinson G. The different baryonic Tully-Fisher relations at low masses. Mon Not R Astron Soc. 2016;459(1):638-645doi: 10.1093/mnras/stw650.
Brook, C. B., Santos-Santos, I., & Stinson, G. (2016). The different baryonic Tully-Fisher relations at low masses. Monthly notices of the Royal Astronomical Society, 459(1), 638-645. https://doi.org/10.1093/mnras/stw650
Brook, Chris B, et al. "The different baryonic Tully-Fisher relations at low masses." Monthly notices of the Royal Astronomical Society vol. 459,1 (2016): 638-645. doi: https://doi.org/10.1093/mnras/stw650
Brook CB, Santos-Santos I, Stinson G. The different baryonic Tully-Fisher relations at low masses. Mon Not R Astron Soc. 2016 Mar 17;459(1):638-645. doi: 10.1093/mnras/stw650. eCollection 2016 Jun 11. PMID: 27274704.
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A POPULATION OF STAURASTRUM FREEMANII FROM THE CENTRAL HIGHLANDS OF NEW GUINEA.

Journal of phycology

Brook AJ, Hine AE.
PMID: 27053317
J Phycol. 1966 Jun;2(2):66-73. doi: 10.1111/j.1529-8817.1966.tb04596.x.

An abundant gathering of the desmid Staurastrum freemanii has been collected from a pond located in the highlands of New Guinea. This material shows considerable polymorphism and contains a number of significant dichotypic forms. Examination of this material questions...

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Brook AJ, Hine AE. A POPULATION OF STAURASTRUM FREEMANII FROM THE CENTRAL HIGHLANDS OF NEW GUINEA. J Phycol. 1966;2(2):66-73doi: 10.1111/j.1529-8817.1966.tb04596.x.
Brook, A. J., & Hine, A. E. (1966). A POPULATION OF STAURASTRUM FREEMANII FROM THE CENTRAL HIGHLANDS OF NEW GUINEA. Journal of phycology, 2(2), 66-73. https://doi.org/10.1111/j.1529-8817.1966.tb04596.x
Brook, A J, and Hine, A E. "A POPULATION OF STAURASTRUM FREEMANII FROM THE CENTRAL HIGHLANDS OF NEW GUINEA." Journal of phycology vol. 2,2 (1966): 66-73. doi: https://doi.org/10.1111/j.1529-8817.1966.tb04596.x
Brook AJ, Hine AE. A POPULATION OF STAURASTRUM FREEMANII FROM THE CENTRAL HIGHLANDS OF NEW GUINEA. J Phycol. 1966 Jun;2(2):66-73. doi: 10.1111/j.1529-8817.1966.tb04596.x. PMID: 27053317.
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Meeting Report of the Fifth International Cancer Epigenetics Conference in Beijing, China, October 2016.

Epigenomics

Gao D, Herman JG, Cui H, Jen J, Fuks F, Brock MV, Ushijima T, Croce C, Akiyama Y, Guo M.
PMID: 28530839
Epigenomics. 2017 Jul;9(7):937-941. doi: 10.2217/epi-2017-0030. Epub 2017 May 22.

Fifth International Cancer Epigenetics Conference, Beijing, China, 21-23 October 2016 This meeting reported many new findings in the field of cancer epigenetics, including basic science, translational and clinical studies. In this report, we summarize some of the main advancements...

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Gao D, Herman JG, Cui H, et al. Meeting Report of the Fifth International Cancer Epigenetics Conference in Beijing, China, October 2016. Epigenomics. 2017;9(7):937-941doi: 10.2217/epi-2017-0030.
Gao, D., Herman, J. G., Cui, H., Jen, J., Fuks, F., Brock, M. V., Ushijima, T., Croce, C., Akiyama, Y., & Guo, M. (2017). Meeting Report of the Fifth International Cancer Epigenetics Conference in Beijing, China, October 2016. Epigenomics, 9(7), 937-941. https://doi.org/10.2217/epi-2017-0030
Gao, Dan, et al. "Meeting Report of the Fifth International Cancer Epigenetics Conference in Beijing, China, October 2016." Epigenomics vol. 9,7 (2017): 937-941. doi: https://doi.org/10.2217/epi-2017-0030
Gao D, Herman JG, Cui H, Jen J, Fuks F, Brock MV, Ushijima T, Croce C, Akiyama Y, Guo M. Meeting Report of the Fifth International Cancer Epigenetics Conference in Beijing, China, October 2016. Epigenomics. 2017 Jul;9(7):937-941. doi: 10.2217/epi-2017-0030. Epub 2017 May 22. PMID: 28530839.
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Oxidation of Electron Donor-Substituted Verdazyls: Building Blocks for Molecular Switches.

The journal of physical chemistry. A

Haller BC, Chambers D, Cheng R, Chemistruck V, Hom TF, Li Z, Nguyen J, Ichimura A, Brook DJ.
PMID: 26451688
J Phys Chem A. 2015 Oct 29;119(43):10750-60. doi: 10.1021/acs.jpca.5b09295. Epub 2015 Oct 20.

Species that can undergo changes in electronic configuration as a result of an external stimulus such as pH or solvent polarity can play an important role in sensors, conducting polymers, and molecular switches. One way to achieve such structures...

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Haller BC, Chambers D, Cheng R, et al. Oxidation of Electron Donor-Substituted Verdazyls: Building Blocks for Molecular Switches. J Phys Chem A. 2015;119(43):10750-60doi: 10.1021/acs.jpca.5b09295.
Haller, B. C., Chambers, D., Cheng, R., Chemistruck, V., Hom, T. F., Li, Z., Nguyen, J., Ichimura, A., & Brook, D. J. (2015). Oxidation of Electron Donor-Substituted Verdazyls: Building Blocks for Molecular Switches. The journal of physical chemistry. A, 119(43), 10750-60. https://doi.org/10.1021/acs.jpca.5b09295
Haller, Benjamin C, et al. "Oxidation of Electron Donor-Substituted Verdazyls: Building Blocks for Molecular Switches." The journal of physical chemistry. A vol. 119,43 (2015): 10750-60. doi: https://doi.org/10.1021/acs.jpca.5b09295
Haller BC, Chambers D, Cheng R, Chemistruck V, Hom TF, Li Z, Nguyen J, Ichimura A, Brook DJ. Oxidation of Electron Donor-Substituted Verdazyls: Building Blocks for Molecular Switches. J Phys Chem A. 2015 Oct 29;119(43):10750-60. doi: 10.1021/acs.jpca.5b09295. Epub 2015 Oct 20. PMID: 26451688.
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Corrigendum: Airway and Parenchymal Strains during Bronchoconstriction in the Precision Cut Lung Slice.

Frontiers in physiology

Hiorns JE, Bidan CM, Jensen OE, Gosens R, Kistemaker LE, Fredberg JJ, Butler JP, Krishnan R, Brook BS.
PMID: 28261114
Front Physiol. 2017 Feb 28;8:117. doi: 10.3389/fphys.2017.00117. eCollection 2017.

[This corrects the article on p. 309 in vol. 7, PMID: 27559314.].

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Hiorns JE, Bidan CM, Jensen OE, et al. Corrigendum: Airway and Parenchymal Strains during Bronchoconstriction in the Precision Cut Lung Slice. Front Physiol. 2017;8:117doi: 10.3389/fphys.2017.00117.
Hiorns, J. E., Bidan, C. M., Jensen, O. E., Gosens, R., Kistemaker, L. E., Fredberg, J. J., Butler, J. P., Krishnan, R., & Brook, B. S. (2017). Corrigendum: Airway and Parenchymal Strains during Bronchoconstriction in the Precision Cut Lung Slice. Frontiers in physiology, 8117. https://doi.org/10.3389/fphys.2017.00117
Hiorns, Jonathan E, et al. "Corrigendum: Airway and Parenchymal Strains during Bronchoconstriction in the Precision Cut Lung Slice." Frontiers in physiology vol. 8 (2017): 117. doi: https://doi.org/10.3389/fphys.2017.00117
Hiorns JE, Bidan CM, Jensen OE, Gosens R, Kistemaker LE, Fredberg JJ, Butler JP, Krishnan R, Brook BS. Corrigendum: Airway and Parenchymal Strains during Bronchoconstriction in the Precision Cut Lung Slice. Front Physiol. 2017 Feb 28;8:117. doi: 10.3389/fphys.2017.00117. eCollection 2017. PMID: 28261114; PMCID: PMC5329043.
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Production of immobilized penicillin acylase using aqueous polymer systems for enzyme purification and in situ immobilization.

Enzyme and microbial technology

Guan YH, Lilley TH, Brook AH.
PMID: 11166815
Enzyme Microb Technol. 2001 Feb 01;28(2):218-224. doi: 10.1016/s0141-0229(00)00305-7.

A novel approach for the isolation and purification of penicillin acylase (PA), which couples aqueous two-phase partitioning and enzyme immobilization has been investigated.A PA yield of 90% was achieved by treating E. coli cells with 4% butyl acetate, freeze-thawing...

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Guan YH, Lilley TH, Brook AH. Production of immobilized penicillin acylase using aqueous polymer systems for enzyme purification and in situ immobilization. Enzyme Microb Technol. 2001;28(2):218-224doi: 10.1016/s0141-0229(00)00305-7.
Guan, Y. H., Lilley, T. H., & Brook, A. H. (2001). Production of immobilized penicillin acylase using aqueous polymer systems for enzyme purification and in situ immobilization. Enzyme and microbial technology, 28(2), 218-224. https://doi.org/10.1016/s0141-0229(00)00305-7
Guan, Y H., et al. "Production of immobilized penicillin acylase using aqueous polymer systems for enzyme purification and in situ immobilization." Enzyme and microbial technology vol. 28,2 (2001): 218-224. doi: https://doi.org/10.1016/s0141-0229(00)00305-7
Guan YH, Lilley TH, Brook AH. Production of immobilized penicillin acylase using aqueous polymer systems for enzyme purification and in situ immobilization. Enzyme Microb Technol. 2001 Feb 01;28(2):218-224. doi: 10.1016/s0141-0229(00)00305-7. PMID: 11166815.
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The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2 Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, a NIH Postdoctoral Fellowship to C.S.B., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the .

Angewandte Chemie (International ed. in English)

Smith III AB, Lin Q, Doughty VA, Zhuang L, McBriar MD, Kerns JK, Brook CS, Murase N, Nakayama K.
PMID: 11169711
Angew Chem Int Ed Engl. 2001 Jan 05;40(1):196-199.

No abstract available.

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Smith III AB, Lin Q, Doughty VA, et al. The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2 Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, a NIH Postdoctoral Fellowship to C.S.B., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the . Angew Chem Int Ed Engl. 2001;40(1):196-199
Smith III, A. B., Lin, Q., Doughty, V. A., Zhuang, L., McBriar, M. D., Kerns, J. K., Brook, C. S., Murase, N., & Nakayama, K. (2001). The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2 Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, a NIH Postdoctoral Fellowship to C.S.B., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the . Angewandte Chemie (International ed. in English), 40(1), 196-199.
Smith III, Amos B., et al. "The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2 Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, a NIH Postdoctoral Fellowship to C.S.B., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the ." Angewandte Chemie (International ed. in English) vol. 40,1 (2001): 196-199.
Smith III AB, Lin Q, Doughty VA, Zhuang L, McBriar MD, Kerns JK, Brook CS, Murase N, Nakayama K. The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2 Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, a NIH Postdoctoral Fellowship to C.S.B., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the . Angew Chem Int Ed Engl. 2001 Jan 05;40(1):196-199. PMID: 11169711.
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Chronic Renal Disease Associated with HIV Infection.

Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia

Holden BM, Brook MG.
PMID: 18209430
Saudi J Kidney Dis Transpl. 2002 Jul-Sep;13(3):344-52.

To describe current knowledge on the etiology, pathology, diagnosis and treatment of HIV-associated nephropathy (HIVAN), a Medline search was performed from 1989 to March 2002 using the key words, "HIV", "nephropathy", "renal" and "kidney". A further search was performed...

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Holden BM, Brook MG. Chronic Renal Disease Associated with HIV Infection. Saudi J Kidney Dis Transpl. 2002;13(3):344-52
Holden, B. M., & Brook, M. G. (2002). Chronic Renal Disease Associated with HIV Infection. Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia, 13(3), 344-52.
Holden, Benedict M, and Brook, M Gary. "Chronic Renal Disease Associated with HIV Infection." Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia vol. 13,3 (2002): 344-52.
Holden BM, Brook MG. Chronic Renal Disease Associated with HIV Infection. Saudi J Kidney Dis Transpl. 2002 Jul-Sep;13(3):344-52. PMID: 18209430.
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