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Showing 13 to 24 of 2623 entries
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Current approaches and advance in mantle cell lymphoma treatment.

Stem cell investigation

Liu Y, Zhang X, Zhong JF.
PMID: 27358886
Stem Cell Investig. 2015 Sep 29;2:18. doi: 10.3978/j.issn.2306-9759.2015.09.02. eCollection 2015.

Mantle cell lymphoma (MCL) is a set of heterogeneous non-Hodgkin lymphoma characterized by involvement of lymph nodes, spleen, bone marrow and blood. Under conventional treatment, survival time is 4 to 5 years with short remission period and there is...

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Liu Y, Zhang X, Zhong JF. Current approaches and advance in mantle cell lymphoma treatment. Stem Cell Investig. 2015;2:18doi: 10.3978/j.issn.2306-9759.2015.09.02.
Liu, Y., Zhang, X., & Zhong, J. F. (2015). Current approaches and advance in mantle cell lymphoma treatment. Stem cell investigation, 218. https://doi.org/10.3978/j.issn.2306-9759.2015.09.02
Liu, Yao, et al. "Current approaches and advance in mantle cell lymphoma treatment." Stem cell investigation vol. 2 (2015): 18. doi: https://doi.org/10.3978/j.issn.2306-9759.2015.09.02
Liu Y, Zhang X, Zhong JF. Current approaches and advance in mantle cell lymphoma treatment. Stem Cell Investig. 2015 Sep 29;2:18. doi: 10.3978/j.issn.2306-9759.2015.09.02. eCollection 2015. PMID: 27358886; PMCID: PMC4923656.
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H.P. Acthar Gel (repository corticotropin injection) treatment of patients with multiple sclerosis and diabetes.

Therapeutic advances in chronic disease

Kutz C.
PMID: 27433309
Ther Adv Chronic Dis. 2016 Jul;7(4):190-7. doi: 10.1177/2040622316644481. Epub 2016 Jun 10.

BACKGROUND: Treatment of multiple sclerosis (MS) relapses can be complex in patients with concomitant diabetes. Corticosteroids and adrenocorticotropic hormones are known to cause alterations in glucose tolerance. Many patients have poor tolerability to therapy, necessitating alternative treatment options. Adrenocorticotropic...

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Kutz C. H.P. Acthar Gel (repository corticotropin injection) treatment of patients with multiple sclerosis and diabetes. Ther Adv Chronic Dis. 2016;7(4):190-7doi: 10.1177/2040622316644481.
Kutz, C. (2016). H.P. Acthar Gel (repository corticotropin injection) treatment of patients with multiple sclerosis and diabetes. Therapeutic advances in chronic disease, 7(4), 190-7. https://doi.org/10.1177/2040622316644481
Kutz, Christen. "H.P. Acthar Gel (repository corticotropin injection) treatment of patients with multiple sclerosis and diabetes." Therapeutic advances in chronic disease vol. 7,4 (2016): 190-7. doi: https://doi.org/10.1177/2040622316644481
Kutz C. H.P. Acthar Gel (repository corticotropin injection) treatment of patients with multiple sclerosis and diabetes. Ther Adv Chronic Dis. 2016 Jul;7(4):190-7. doi: 10.1177/2040622316644481. Epub 2016 Jun 10. PMID: 27433309; PMCID: PMC4935834.
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Repository corticotropin injection in a patient presenting with focal segmental glomerulosclerosis, rheumatoid arthritis, and optic neuritis: a case report.

International journal of general medicine

Madan A.
PMID: 25848316
Int J Gen Med. 2015 Mar 20;8:119-24. doi: 10.2147/IJGM.S79815. eCollection 2015.

BACKGROUND: Focal segmental glomerulosclerosis (FSGS) causes scarring or sclerosis of glomeruli that act as tiny filters in the kidneys, damage to which results in diminished ability to properly filter blood, resulting in the urinary loss of plasma proteins and...

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Madan A. Repository corticotropin injection in a patient presenting with focal segmental glomerulosclerosis, rheumatoid arthritis, and optic neuritis: a case report. Int J Gen Med. 2015;8:119-24doi: 10.2147/IJGM.S79815.
Madan, A. (2015). Repository corticotropin injection in a patient presenting with focal segmental glomerulosclerosis, rheumatoid arthritis, and optic neuritis: a case report. International journal of general medicine, 8119-24. https://doi.org/10.2147/IJGM.S79815
Madan, Arvind. "Repository corticotropin injection in a patient presenting with focal segmental glomerulosclerosis, rheumatoid arthritis, and optic neuritis: a case report." International journal of general medicine vol. 8 (2015): 119-24. doi: https://doi.org/10.2147/IJGM.S79815
Madan A. Repository corticotropin injection in a patient presenting with focal segmental glomerulosclerosis, rheumatoid arthritis, and optic neuritis: a case report. Int J Gen Med. 2015 Mar 20;8:119-24. doi: 10.2147/IJGM.S79815. eCollection 2015. PMID: 25848316; PMCID: PMC4374712.
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Pyoderma Gangrenosum Simulating Necrotizing Fasciitis.

Case reports in medicine

de Souza EF, da Silva GA, Dos Santos GR, Motta HL, Cardoso PA, de Azevedo MC, Pires KL, Motta RN, Eyer Silva Wde A, Ferry FR, Pinto JF.
PMID: 26783395
Case Rep Med. 2015;2015:504970. doi: 10.1155/2015/504970. Epub 2015 Dec 10.

Pyoderma gangrenosum received this name due to the notion that this disease was related to infections caused by bacteria in the genus Streptococcus. In contrast to this initial assumption, today the disease is thought to have an autoimmune origin....

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de Souza EF, da Silva GA, Dos Santos GR, et al. Pyoderma Gangrenosum Simulating Necrotizing Fasciitis. Case Rep Med. 2015;2015:504970doi: 10.1155/2015/504970.
de Souza, E. F., da Silva, G. A., Dos Santos, G. R., Motta, H. L., Cardoso, P. A., de Azevedo, M. C., Pires, K. L., Motta, R. N., Eyer Silva, W. d. e. . A., Ferry, F. R., & Pinto, J. F. (2015). Pyoderma Gangrenosum Simulating Necrotizing Fasciitis. Case reports in medicine, 2015504970. https://doi.org/10.1155/2015/504970
de Souza, Erik Friedrich Alex, et al. "Pyoderma Gangrenosum Simulating Necrotizing Fasciitis." Case reports in medicine vol. 2015 (2015): 504970. doi: https://doi.org/10.1155/2015/504970
de Souza EF, da Silva GA, Dos Santos GR, Motta HL, Cardoso PA, de Azevedo MC, Pires KL, Motta RN, Eyer Silva Wde A, Ferry FR, Pinto JF. Pyoderma Gangrenosum Simulating Necrotizing Fasciitis. Case Rep Med. 2015;2015:504970. doi: 10.1155/2015/504970. Epub 2015 Dec 10. PMID: 26783395; PMCID: PMC4689958.
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THE ACHES THAT TAKE YOUR BREATH (AND TEARS) AWAY.

The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society

Becerril J, Gonzales H, Saketkoo LA.
PMID: 27159479
J La State Med Soc. 2015 May-Jun;167(3):154-5. Epub 2015 Jun 15.

An 80-year-old man presented with a complaint of three months of fatigue and aching of his shoulders and hips, as well as pain, swelling, and stiffness in bilateral fingers that was worse in the morning but improved with movement....

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Becerril J, Gonzales H, Saketkoo LA. THE ACHES THAT TAKE YOUR BREATH (AND TEARS) AWAY. J La State Med Soc. 2015;167(3):154-5
Becerril, J., Gonzales, H., & Saketkoo, L. A. (2015). THE ACHES THAT TAKE YOUR BREATH (AND TEARS) AWAY. The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society, 167(3), 154-5.
Becerril, J, et al. "THE ACHES THAT TAKE YOUR BREATH (AND TEARS) AWAY." The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society vol. 167,3 (2015): 154-5.
Becerril J, Gonzales H, Saketkoo LA. THE ACHES THAT TAKE YOUR BREATH (AND TEARS) AWAY. J La State Med Soc. 2015 May-Jun;167(3):154-5. Epub 2015 Jun 15. PMID: 27159479.
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STILL FEBRILE - A RARE CAUSE OF JOINT PAIN.

The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society

Raley M.
PMID: 27159486
J La State Med Soc. 2015 May-Jun;167(3):158. Epub 2015 Jun 15.

A 35-year-old woman presented to our emergency department complaining of arthralgia, rash, fevers, and muscle weakness for the past year. These symptoms initially began as unilateral upper lip swelling, which then progressed to a facial rash and orbital swelling...

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Raley M. STILL FEBRILE - A RARE CAUSE OF JOINT PAIN. J La State Med Soc. 2015;167(3):158
Raley, M. (2015). STILL FEBRILE - A RARE CAUSE OF JOINT PAIN. The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society, 167(3), 158.
Raley, M. "STILL FEBRILE - A RARE CAUSE OF JOINT PAIN." The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society vol. 167,3 (2015): 158.
Raley M. STILL FEBRILE - A RARE CAUSE OF JOINT PAIN. J La State Med Soc. 2015 May-Jun;167(3):158. Epub 2015 Jun 15. PMID: 27159486.
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On-demand intermittent beclomethasone is effective for mild asthma in Brazil.

Clinical and translational allergy

Camargos P, Affonso A, Calazans G, Ramalho L, Ribeiro ML, Jentzsch N, Senna S, Stein RT.
PMID: 29515802
Clin Transl Allergy. 2018 Mar 05;8:7. doi: 10.1186/s13601-018-0192-0. eCollection 2018.

BACKGROUND: Daily inhaled corticosteroids are widely recommended for mild persistent asthma. This study aimed to assess the efficacy of the intermittent use of beclomethasone as an alternative treatment for mild persistent asthma.METHODS: In this 16-week trial, children aged 6-18...

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Camargos P, Affonso A, Calazans G, et al. On-demand intermittent beclomethasone is effective for mild asthma in Brazil. Clin Transl Allergy. 2018;8:7doi: 10.1186/s13601-018-0192-0.
Camargos, P., Affonso, A., Calazans, G., Ramalho, L., Ribeiro, M. L., Jentzsch, N., Senna, S., & Stein, R. T. (2018). On-demand intermittent beclomethasone is effective for mild asthma in Brazil. Clinical and translational allergy, 87. https://doi.org/10.1186/s13601-018-0192-0
Camargos, Paulo, et al. "On-demand intermittent beclomethasone is effective for mild asthma in Brazil." Clinical and translational allergy vol. 8 (2018): 7. doi: https://doi.org/10.1186/s13601-018-0192-0
Camargos P, Affonso A, Calazans G, Ramalho L, Ribeiro ML, Jentzsch N, Senna S, Stein RT. On-demand intermittent beclomethasone is effective for mild asthma in Brazil. Clin Transl Allergy. 2018 Mar 05;8:7. doi: 10.1186/s13601-018-0192-0. eCollection 2018. PMID: 29515802; PMCID: PMC5836456.
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Acquired pure megakaryocytic aplasia successfully treated with cyclosporine.

Turkish journal of haematology : official journal of Turkish Society of Haematology

Omri HE, Ibrahim F, Taha RY, Negm RH, Khinji AA, Yassin M, Hijji IA, Ayoubi HE, Baden H.
PMID: 27263744
Turk J Haematol. 2010 Dec 05;27(4):289-93. doi: 10.5152/tjh.2010.51.

Acquired pure megakaryocytic aplasia is a rare hematological disorder characterized by thrombocytopenia with absent or markedly reduced megakaryocytes in the bone marrow. We report a case of a 25-year-old male diagnosed as acquired pure megakaryocytic aplasia. Treatment with prednisone...

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Omri HE, Ibrahim F, Taha RY, et al. Siklosporin ile başarılı şekilde tedavi edilen kazanılmış saf megakaryositik aplazi. Acquired pure megakaryocytic aplasia successfully treated with cyclosporine. Turk J Haematol. 2010;27(4):289-93doi: 10.5152/tjh.2010.51.
Omri, H. E., Ibrahim, F., Taha, R. Y., Negm, R. H., Khinji, A. A., Yassin, M., Hijji, I. A., Ayoubi, H. E., & Baden, H. (2010). Siklosporin ile başarılı şekilde tedavi edilen kazanılmış saf megakaryositik aplazi. Acquired pure megakaryocytic aplasia successfully treated with cyclosporine. Turkish journal of haematology : official journal of Turkish Society of Haematology, 27(4), 289-93. https://doi.org/10.5152/tjh.2010.51
Omri, Halima El, et al. "Siklosporin ile başarılı şekilde tedavi edilen kazanılmış saf megakaryositik aplazi." Acquired pure megakaryocytic aplasia successfully treated with cyclosporine. Turkish journal of haematology : official journal of Turkish Society of Haematology vol. 27,4 (2010): 289-93. doi: https://doi.org/10.5152/tjh.2010.51
Omri HE, Ibrahim F, Taha RY, Negm RH, Khinji AA, Yassin M, Hijji IA, Ayoubi HE, Baden H. Siklosporin ile başarılı şekilde tedavi edilen kazanılmış saf megakaryositik aplazi. Acquired pure megakaryocytic aplasia successfully treated with cyclosporine. Turk J Haematol. 2010 Dec 05;27(4):289-93. doi: 10.5152/tjh.2010.51. PMID: 27263744.
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Cryoglobulinemic membranoproliferative glomerulonephritis associated with mucosa-associated lymphoid tissue lymphoma treated with rituximab.

Clinical nephrology. Case studies

Ha AY, Noronha N, Gleason P, Winkler JN, Butera JN, Henriksen KJ, Hu SL.
PMID: 29043134
Clin Nephrol Case Stud. 2016 Jan 19;4:1-4. doi: 10.5414/CNCS108740. eCollection 2016.

Cryoglobulinemia and mucosa-associated lymphoid tissue (MALT) lymphoma are diseases characterized by B-cell dysregulation and overproduction of antibodies. Vasculitis and cutaneous manifestations are common, but renal involvement is rare. A 65-year-old woman with type 1 cryoglobulinemia and MALT lymphomas of...

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Ha AY, Noronha N, Gleason P, et al. Cryoglobulinemic membranoproliferative glomerulonephritis associated with mucosa-associated lymphoid tissue lymphoma treated with rituximab. Clin Nephrol Case Stud. 2016;4:1-4doi: 10.5414/CNCS108740.
Ha, A. Y., Noronha, N., Gleason, P., Winkler, J. N., Butera, J. N., Henriksen, K. J., & Hu, S. L. (2016). Cryoglobulinemic membranoproliferative glomerulonephritis associated with mucosa-associated lymphoid tissue lymphoma treated with rituximab. Clinical nephrology. Case studies, 41-4. https://doi.org/10.5414/CNCS108740
Ha, Austin Y, et al. "Cryoglobulinemic membranoproliferative glomerulonephritis associated with mucosa-associated lymphoid tissue lymphoma treated with rituximab." Clinical nephrology. Case studies vol. 4 (2016): 1-4. doi: https://doi.org/10.5414/CNCS108740
Ha AY, Noronha N, Gleason P, Winkler JN, Butera JN, Henriksen KJ, Hu SL. Cryoglobulinemic membranoproliferative glomerulonephritis associated with mucosa-associated lymphoid tissue lymphoma treated with rituximab. Clin Nephrol Case Stud. 2016 Jan 19;4:1-4. doi: 10.5414/CNCS108740. eCollection 2016. PMID: 29043134; PMCID: PMC5437996.
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Benign acute childhood myositis complicating influenza B infection in a boy with idiopathic nephrotic syndrome.

Central-European journal of immunology

Skrzypczyk P, Przychodzień J, Pańczyk-Tomaszewska M.
PMID: 27833453
Cent Eur J Immunol. 2016;41(3):328-331. doi: 10.5114/ceji.2016.63135. Epub 2016 Oct 25.

INTRODUCTION: Benign acute childhood myositis (BACM) is an acute complication of an infection characterized by calf pain, limitation of lower limb mobility, an increase in serum creatine kinase, and a self-limiting course. No reports of BACM in children with...

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Skrzypczyk P, Przychodzień J, Pańczyk-Tomaszewska M. Benign acute childhood myositis complicating influenza B infection in a boy with idiopathic nephrotic syndrome. Cent Eur J Immunol. 2016;41(3):328-331doi: 10.5114/ceji.2016.63135.
Skrzypczyk, P., Przychodzień, J., & Pańczyk-Tomaszewska, M. (2016). Benign acute childhood myositis complicating influenza B infection in a boy with idiopathic nephrotic syndrome. Central-European journal of immunology, 41(3), 328-331. https://doi.org/10.5114/ceji.2016.63135
Skrzypczyk, Piotr, et al. "Benign acute childhood myositis complicating influenza B infection in a boy with idiopathic nephrotic syndrome." Central-European journal of immunology vol. 41,3 (2016): 328-331. doi: https://doi.org/10.5114/ceji.2016.63135
Skrzypczyk P, Przychodzień J, Pańczyk-Tomaszewska M. Benign acute childhood myositis complicating influenza B infection in a boy with idiopathic nephrotic syndrome. Cent Eur J Immunol. 2016;41(3):328-331. doi: 10.5114/ceji.2016.63135. Epub 2016 Oct 25. PMID: 27833453; PMCID: PMC5099392.
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Response to Paclitaxel in an Adult Patient with Advanced Kaposiform Hemangioendothelioma.

Case reports in oncology

Mota JM, Scaranti M, Fonseca LG, Tolói DA, de Camargo VP, Munhoz RR, Feher O, Hoff PM.
PMID: 27721772
Case Rep Oncol. 2016 Aug 24;9(2):481-487. doi: 10.1159/000448111. eCollection 2016.

BACKGROUND: Kaposiform hemangioendothelioma (KHE) is a rare neoplasm of vascular origin that typically arises from the skin or soft tissues as a solitary tumor. The optimal therapy for this disease is still unknown. We report the case of an...

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Mota JM, Scaranti M, Fonseca LG, et al. Response to Paclitaxel in an Adult Patient with Advanced Kaposiform Hemangioendothelioma. Case Rep Oncol. 2016;9(2):481-487doi: 10.1159/000448111.
Mota, J. M., Scaranti, M., Fonseca, L. G., Tolói, D. A., de Camargo, V. P., Munhoz, R. R., Feher, O., & Hoff, P. M. (2016). Response to Paclitaxel in an Adult Patient with Advanced Kaposiform Hemangioendothelioma. Case reports in oncology, 9(2), 481-487. https://doi.org/10.1159/000448111
Mota, José Maurício, et al. "Response to Paclitaxel in an Adult Patient with Advanced Kaposiform Hemangioendothelioma." Case reports in oncology vol. 9,2 (2016): 481-487. doi: https://doi.org/10.1159/000448111
Mota JM, Scaranti M, Fonseca LG, Tolói DA, de Camargo VP, Munhoz RR, Feher O, Hoff PM. Response to Paclitaxel in an Adult Patient with Advanced Kaposiform Hemangioendothelioma. Case Rep Oncol. 2016 Aug 24;9(2):481-487. doi: 10.1159/000448111. eCollection 2016. PMID: 27721772; PMCID: PMC5043218.
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Levamisole therapy in children with frequently relapsing and steroid-dependent nephrotic syndrome: a single-center experience.

Central-European journal of immunology

Kuźma-Mroczkowska E, Skrzypczyk P, Pańczyk-Tomaszewska M.
PMID: 27833440
Cent Eur J Immunol. 2016;41(3):243-247. doi: 10.5114/ceji.2016.63122. Epub 2016 Oct 25.

INTRODUCTION: Numerous studies suggest that levamisole, an antihelmintic agent with an immunomodulatory effect, reduces the number of relapses in children with frequently relapsing and steroid-dependent nephrotic syndrome (FRNS/SDNS). The aim of the study was to present a single center's...

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Kuźma-Mroczkowska E, Skrzypczyk P, Pańczyk-Tomaszewska M. Levamisole therapy in children with frequently relapsing and steroid-dependent nephrotic syndrome: a single-center experience. Cent Eur J Immunol. 2016;41(3):243-247doi: 10.5114/ceji.2016.63122.
Kuźma-Mroczkowska, E., Skrzypczyk, P., & Pańczyk-Tomaszewska, M. (2016). Levamisole therapy in children with frequently relapsing and steroid-dependent nephrotic syndrome: a single-center experience. Central-European journal of immunology, 41(3), 243-247. https://doi.org/10.5114/ceji.2016.63122
Kuźma-Mroczkowska, Elżbieta, et al. "Levamisole therapy in children with frequently relapsing and steroid-dependent nephrotic syndrome: a single-center experience." Central-European journal of immunology vol. 41,3 (2016): 243-247. doi: https://doi.org/10.5114/ceji.2016.63122
Kuźma-Mroczkowska E, Skrzypczyk P, Pańczyk-Tomaszewska M. Levamisole therapy in children with frequently relapsing and steroid-dependent nephrotic syndrome: a single-center experience. Cent Eur J Immunol. 2016;41(3):243-247. doi: 10.5114/ceji.2016.63122. Epub 2016 Oct 25. PMID: 27833440; PMCID: PMC5099379.
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Showing 13 to 24 of 2623 entries