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Showing 1 to 12 of 2998 entries
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Systemic steroid application caused sudden death of a patient with sudden deafness.

Case reports in otolaryngology

Ogino-Nishimura E, Nakagawa T, Tateya I, Hiraumi H, Ito J.
PMID: 23476857
Case Rep Otolaryngol. 2013;2013:734131. doi: 10.1155/2013/734131. Epub 2013 Feb 11.

A 63-year-old man, who was diagnosed with sudden sensorineural hearing loss (SSHL), showed severe hypertension 10 hours after prednisolone administration. Subsequently, the patient suddenly died due to pulmonary edema. The autopsy indicated a pheochromocytoma in the right adrenal gland,...

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Ogino-Nishimura E, Nakagawa T, Tateya I, et al. Systemic steroid application caused sudden death of a patient with sudden deafness. Case Rep Otolaryngol. 2013;2013:734131doi: 10.1155/2013/734131.
Ogino-Nishimura, E., Nakagawa, T., Tateya, I., Hiraumi, H., & Ito, J. (2013). Systemic steroid application caused sudden death of a patient with sudden deafness. Case reports in otolaryngology, 2013734131. https://doi.org/10.1155/2013/734131
Ogino-Nishimura, Eriko, et al. "Systemic steroid application caused sudden death of a patient with sudden deafness." Case reports in otolaryngology vol. 2013 (2013): 734131. doi: https://doi.org/10.1155/2013/734131
Ogino-Nishimura E, Nakagawa T, Tateya I, Hiraumi H, Ito J. Systemic steroid application caused sudden death of a patient with sudden deafness. Case Rep Otolaryngol. 2013;2013:734131. doi: 10.1155/2013/734131. Epub 2013 Feb 11. PMID: 23476857; PMCID: PMC3582076.
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Bilateral corticosteroid-induced osteonecrosis of the femoral head detected at a 6-week interval.

SpringerPlus

Sonoda K, Yamamoto T, Motomura G, Hamai S, Karasuyama K, Kubo Y, Iwamoto Y.
PMID: 26558165
Springerplus. 2015 Nov 02;4:662. doi: 10.1186/s40064-015-1458-9. eCollection 2015.

INTRODUCTION: Corticosteroid-induced osteonecrosis of the femoral head (ONFH) often affects both femoral heads. Such bilateral ONFH cases are generally detected concurrently on magnetic resonance imaging (MRI). On the other hand, in unilateral cases, it is rare that contralateral ONFH...

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Sonoda K, Yamamoto T, Motomura G, et al. Bilateral corticosteroid-induced osteonecrosis of the femoral head detected at a 6-week interval. Springerplus. 2015;4:662doi: 10.1186/s40064-015-1458-9.
Sonoda, K., Yamamoto, T., Motomura, G., Hamai, S., Karasuyama, K., Kubo, Y., & Iwamoto, Y. (2015). Bilateral corticosteroid-induced osteonecrosis of the femoral head detected at a 6-week interval. SpringerPlus, 4662. https://doi.org/10.1186/s40064-015-1458-9
Sonoda, Kazuhiko, et al. "Bilateral corticosteroid-induced osteonecrosis of the femoral head detected at a 6-week interval." SpringerPlus vol. 4 (2015): 662. doi: https://doi.org/10.1186/s40064-015-1458-9
Sonoda K, Yamamoto T, Motomura G, Hamai S, Karasuyama K, Kubo Y, Iwamoto Y. Bilateral corticosteroid-induced osteonecrosis of the femoral head detected at a 6-week interval. Springerplus. 2015 Nov 02;4:662. doi: 10.1186/s40064-015-1458-9. eCollection 2015. PMID: 26558165; PMCID: PMC4630241.
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Phacoemulsification versus small incision cataract surgery in patients with uveitis.

International journal of ophthalmology

Bhargava R, Kumar P, Sharma SK, Kumar M, Kaur A.
PMID: 26558210
Int J Ophthalmol. 2015 Oct 18;8(5):965-70. doi: 10.3980/j.issn.2222-3959.2015.05.20. eCollection 2015.

AIM: To compare the safety and efficacy of phacoemulsification and small incision cataract surgery (SICS) in patients with uveitic cataract.METHODS: In a prospective, randomized multi-centric study, consecutive patients with uveitic cataract were randomized to receive phacoemulsification or manual SICS...

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Bhargava R, Kumar P, Sharma SK, et al. Phacoemulsification versus small incision cataract surgery in patients with uveitis. Int J Ophthalmol. 2015;8(5):965-70doi: 10.3980/j.issn.2222-3959.2015.05.20.
Bhargava, R., Kumar, P., Sharma, S. K., Kumar, M., & Kaur, A. (2015). Phacoemulsification versus small incision cataract surgery in patients with uveitis. International journal of ophthalmology, 8(5), 965-70. https://doi.org/10.3980/j.issn.2222-3959.2015.05.20
Bhargava, Rahul, et al. "Phacoemulsification versus small incision cataract surgery in patients with uveitis." International journal of ophthalmology vol. 8,5 (2015): 965-70. doi: https://doi.org/10.3980/j.issn.2222-3959.2015.05.20
Bhargava R, Kumar P, Sharma SK, Kumar M, Kaur A. Phacoemulsification versus small incision cataract surgery in patients with uveitis. Int J Ophthalmol. 2015 Oct 18;8(5):965-70. doi: 10.3980/j.issn.2222-3959.2015.05.20. eCollection 2015. PMID: 26558210; PMCID: PMC4630994.
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Acute Hemorrhagic Edema of Infancy: an unusual diagnosis for the general pediatrician.

Autopsy & case reports

Cunha DF, Darcie AL, Benevides GN, Ferronato AE, Hein N, Lo DS, Yoshioka CR, Hirose M, Cardoso DM, Gilio AE.
PMID: 26558246
Autops Case Rep. 2015 Sep 30;5(3):37-41. doi: 10.4322/acr.2015.020. eCollection 2015.

Acute Hemorrhagic Edema of Infancy (AHEI) is a rare leukocytoclastic vasculitis, clinically characterized by the classical triad: palpable purpuric skin lesions, edema and fever, and is commonly misdiagnosed as Henoch-Schönlein purpura. In addition to its sudden onset, AHEI is...

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Cunha DF, Darcie AL, Benevides GN, et al. Acute Hemorrhagic Edema of Infancy: an unusual diagnosis for the general pediatrician. Autops Case Rep. 2015;5(3):37-41doi: 10.4322/acr.2015.020.
Cunha, D. F., Darcie, A. L., Benevides, G. N., Ferronato, A. E., Hein, N., Lo, D. S., Yoshioka, C. R., Hirose, M., Cardoso, D. M., & Gilio, A. E. (2015). Acute Hemorrhagic Edema of Infancy: an unusual diagnosis for the general pediatrician. Autopsy & case reports, 5(3), 37-41. https://doi.org/10.4322/acr.2015.020
Cunha, Diego Fontana Siqueira, et al. "Acute Hemorrhagic Edema of Infancy: an unusual diagnosis for the general pediatrician." Autopsy & case reports vol. 5,3 (2015): 37-41. doi: https://doi.org/10.4322/acr.2015.020
Cunha DF, Darcie AL, Benevides GN, Ferronato AE, Hein N, Lo DS, Yoshioka CR, Hirose M, Cardoso DM, Gilio AE. Acute Hemorrhagic Edema of Infancy: an unusual diagnosis for the general pediatrician. Autops Case Rep. 2015 Sep 30;5(3):37-41. doi: 10.4322/acr.2015.020. eCollection 2015. PMID: 26558246; PMCID: PMC4636105.
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Colon Mucosa Exhibits Loss of Ectopic MUC5AC Expression in Patients with Ulcerative Colitis Treated with Oral Tacrolimus.

ISRN gastroenterology

Mizoshita T, Tanida S, Tsukamoto H, Ozeki K, Katano T, Ebi M, Mori Y, Kataoka H, Kamiya T, Joh T.
PMID: 23691335
ISRN Gastroenterol. 2013 Apr 09;2013:304894. doi: 10.1155/2013/304894. Print 2013.

Background. Tacrolimus (FK506) is effective for patients with ulcerative colitis (UC). However, there are few reports on tacrolimus therapy (TT) with respect to the relationship with endoscopic and clinicopathologic findings. Methods. Thirty patients with moderate/severe active UC refractory to...

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Mizoshita T, Tanida S, Tsukamoto H, et al. Colon Mucosa Exhibits Loss of Ectopic MUC5AC Expression in Patients with Ulcerative Colitis Treated with Oral Tacrolimus. ISRN Gastroenterol. 2013;2013:304894doi: 10.1155/2013/304894.
Mizoshita, T., Tanida, S., Tsukamoto, H., Ozeki, K., Katano, T., Ebi, M., Mori, Y., Kataoka, H., Kamiya, T., & Joh, T. (2013). Colon Mucosa Exhibits Loss of Ectopic MUC5AC Expression in Patients with Ulcerative Colitis Treated with Oral Tacrolimus. ISRN gastroenterology, 2013304894. https://doi.org/10.1155/2013/304894
Mizoshita, Tsutomu, et al. "Colon Mucosa Exhibits Loss of Ectopic MUC5AC Expression in Patients with Ulcerative Colitis Treated with Oral Tacrolimus." ISRN gastroenterology vol. 2013 (2013): 304894. doi: https://doi.org/10.1155/2013/304894
Mizoshita T, Tanida S, Tsukamoto H, Ozeki K, Katano T, Ebi M, Mori Y, Kataoka H, Kamiya T, Joh T. Colon Mucosa Exhibits Loss of Ectopic MUC5AC Expression in Patients with Ulcerative Colitis Treated with Oral Tacrolimus. ISRN Gastroenterol. 2013 Apr 09;2013:304894. doi: 10.1155/2013/304894. Print 2013. PMID: 23691335; PMCID: PMC3649514.
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Kidney Transplant in a Human Immunodeficiency Virus-Positive Patient: Case Report of Drug Interactions.

Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation

Yılmaz M, Gökengin D, Bozbıyık O, Hoşcoşkun C, Uyan A, Töz H.
PMID: 28969531
Exp Clin Transplant. 2017 Sep 30; doi: 10.6002/ect.2017.0013. Epub 2017 Sep 30.

End-stage renal disease in the human immunodeficiency virus-positive population is increasing. Kidney transplant is the optimal therapy for this population rather than dialysis modalities if some criteria are met. These include undetectable plasma human immunodeficiency virus RNA, CD4 cell...

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Yılmaz M, Gökengin D, Bozbıyık O, et al. Kidney Transplant in a Human Immunodeficiency Virus-Positive Patient: Case Report of Drug Interactions. Exp Clin Transplant. 2017;doi: 10.6002/ect.2017.0013.
Yılmaz, M., Gökengin, D., Bozbıyık, O., Hoşcoşkun, C., Uyan, A., & Töz, H. (2017). Kidney Transplant in a Human Immunodeficiency Virus-Positive Patient: Case Report of Drug Interactions. Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, . https://doi.org/10.6002/ect.2017.0013
Yılmaz, Mümtaz, et al. "Kidney Transplant in a Human Immunodeficiency Virus-Positive Patient: Case Report of Drug Interactions." Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation vol. (2017). doi: https://doi.org/10.6002/ect.2017.0013
Yılmaz M, Gökengin D, Bozbıyık O, Hoşcoşkun C, Uyan A, Töz H. Kidney Transplant in a Human Immunodeficiency Virus-Positive Patient: Case Report of Drug Interactions. Exp Clin Transplant. 2017 Sep 30; doi: 10.6002/ect.2017.0013. Epub 2017 Sep 30. PMID: 28969531.
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Cutaneous leukocytoclastic vasculitis: the role of lymphocytes and related immune markers.

Postepy dermatologii i alergologii

Gambichler T, Kulik MA, Skrygan M, Rooms I, Höxtermann S.
PMID: 28951703
Postepy Dermatol Alergol. 2017 Aug;34(4):299-305. doi: 10.5114/ada.2017.69307. Epub 2017 Aug 01.

INTRODUCTION: Apart from neutrophils, other immune cells may play a significant pathogenetic role in cutaneous leukocytoclastic vasculitis (CLV).AIM: To investigate lymphocytes and related immunological factors in patients with CLV requiring systemic glucocorticosteroid treatment.MATERIAL AND METHODS: Fourteen patients with severe...

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Gambichler T, Kulik MA, Skrygan M, et al. Cutaneous leukocytoclastic vasculitis: the role of lymphocytes and related immune markers. Postepy Dermatol Alergol. 2017;34(4):299-305doi: 10.5114/ada.2017.69307.
Gambichler, T., Kulik, M. A., Skrygan, M., Rooms, I., & Höxtermann, S. (2017). Cutaneous leukocytoclastic vasculitis: the role of lymphocytes and related immune markers. Postepy dermatologii i alergologii, 34(4), 299-305. https://doi.org/10.5114/ada.2017.69307
Gambichler, Thilo, et al. "Cutaneous leukocytoclastic vasculitis: the role of lymphocytes and related immune markers." Postepy dermatologii i alergologii vol. 34,4 (2017): 299-305. doi: https://doi.org/10.5114/ada.2017.69307
Gambichler T, Kulik MA, Skrygan M, Rooms I, Höxtermann S. Cutaneous leukocytoclastic vasculitis: the role of lymphocytes and related immune markers. Postepy Dermatol Alergol. 2017 Aug;34(4):299-305. doi: 10.5114/ada.2017.69307. Epub 2017 Aug 01. PMID: 28951703; PMCID: PMC5560176.
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Two Cases of Nivolumab Re-Administration after Pneumonitis as Immune-Related Adverse Events.

Case reports in oncology

Imafuku K, Yoshino K, Yamaguchi K, Tsuboi S, Ohara K, Hata H.
PMID: 28512413
Case Rep Oncol. 2017 Apr 04;10(1):296-300. doi: 10.1159/000463379. eCollection 2017.

Nivolumab is a recently approved medication for the treatment of unresectable malignant melanoma. Many immune-related adverse events (irAEs) associated with nivolumab have been reported, such as pneumonitis, hepatitis, dermatitis, and thyroiditis. Prednisolone can effectively treat irAEs. However, it is...

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Imafuku K, Yoshino K, Yamaguchi K, et al. Two Cases of Nivolumab Re-Administration after Pneumonitis as Immune-Related Adverse Events. Case Rep Oncol. 2017;10(1):296-300doi: 10.1159/000463379.
Imafuku, K., Yoshino, K., Yamaguchi, K., Tsuboi, S., Ohara, K., & Hata, H. (2017). Two Cases of Nivolumab Re-Administration after Pneumonitis as Immune-Related Adverse Events. Case reports in oncology, 10(1), 296-300. https://doi.org/10.1159/000463379
Imafuku, Keisuke, et al. "Two Cases of Nivolumab Re-Administration after Pneumonitis as Immune-Related Adverse Events." Case reports in oncology vol. 10,1 (2017): 296-300. doi: https://doi.org/10.1159/000463379
Imafuku K, Yoshino K, Yamaguchi K, Tsuboi S, Ohara K, Hata H. Two Cases of Nivolumab Re-Administration after Pneumonitis as Immune-Related Adverse Events. Case Rep Oncol. 2017 Apr 04;10(1):296-300. doi: 10.1159/000463379. eCollection 2017. PMID: 28512413; PMCID: PMC5422733.
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A case of the "cellular variant" of focal segmental glomerulosclerosis with acute renal failure that remitted completely with oral steroid administration.

CEN case reports

Konno G, Someya G, Sekine K, Nishino T, Kawamoto S.
PMID: 28509069
CEN Case Rep. 2012 Nov;1(2):77-81. doi: 10.1007/s13730-012-0017-2. Epub 2012 Jun 19.

A 73-year-old man with systemic edema and oliguria, which appeared within several days, was referred to our hospital. Urinalysis showed massive proteinuria, and the blood examination results indicated nephrotic syndrome. Renal biopsy revealed the existence of focal segmental glomerulosclerosis...

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Konno G, Someya G, Sekine K, et al. A case of the "cellular variant" of focal segmental glomerulosclerosis with acute renal failure that remitted completely with oral steroid administration. CEN Case Rep. 2012;1(2):77-81doi: 10.1007/s13730-012-0017-2.
Konno, G., Someya, G., Sekine, K., Nishino, T., & Kawamoto, S. (2012). A case of the "cellular variant" of focal segmental glomerulosclerosis with acute renal failure that remitted completely with oral steroid administration. CEN case reports, 1(2), 77-81. https://doi.org/10.1007/s13730-012-0017-2
Konno, Gaku, et al. "A case of the "cellular variant" of focal segmental glomerulosclerosis with acute renal failure that remitted completely with oral steroid administration." CEN case reports vol. 1,2 (2012): 77-81. doi: https://doi.org/10.1007/s13730-012-0017-2
Konno G, Someya G, Sekine K, Nishino T, Kawamoto S. A case of the "cellular variant" of focal segmental glomerulosclerosis with acute renal failure that remitted completely with oral steroid administration. CEN Case Rep. 2012 Nov;1(2):77-81. doi: 10.1007/s13730-012-0017-2. Epub 2012 Jun 19. PMID: 28509069; PMCID: PMC5413643.
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Antithyroid drug-associated MPO-ANCA-positive tubulointerstitial nephritis in a type 2 diabetes patient: a case report.

CEN case reports

Nishimura S, Nakao K, Takeda M, Matsuura I, Nomura Y, Shojima S, Yamamura Y, Fujita K, Momoki N, Maruyama K, Yamamura M, Hiramatsu M.
PMID: 28509121
CEN Case Rep. 2017 May;6(1):22-28. doi: 10.1007/s13730-016-0237-y. Epub 2016 Oct 03.

A 54-year-old man diagnosed with type 2 diabetes and hyperthyroidism was prescribed propylthiouracil (PTU) after the patient developed hepatic dysfunction on thiamazole. At 50 mg/day of PTU, he was stable with thyroid-stimulating hormone receptor and thyrotropic antibody titers remaining...

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Nishimura S, Nakao K, Takeda M, et al. Antithyroid drug-associated MPO-ANCA-positive tubulointerstitial nephritis in a type 2 diabetes patient: a case report. CEN Case Rep. 2016;6(1):22-28doi: 10.1007/s13730-016-0237-y.
Nishimura, S., Nakao, K., Takeda, M., Matsuura, I., Nomura, Y., Shojima, S., Yamamura, Y., Fujita, K., Momoki, N., Maruyama, K., Yamamura, M., & Hiramatsu, M. (2017). Antithyroid drug-associated MPO-ANCA-positive tubulointerstitial nephritis in a type 2 diabetes patient: a case report. CEN case reports, 6(1), 22-28. https://doi.org/10.1007/s13730-016-0237-y
Nishimura, Shinsuke, et al. "Antithyroid drug-associated MPO-ANCA-positive tubulointerstitial nephritis in a type 2 diabetes patient: a case report." CEN case reports vol. 6,1 (2017): 22-28. doi: https://doi.org/10.1007/s13730-016-0237-y
Nishimura S, Nakao K, Takeda M, Matsuura I, Nomura Y, Shojima S, Yamamura Y, Fujita K, Momoki N, Maruyama K, Yamamura M, Hiramatsu M. Antithyroid drug-associated MPO-ANCA-positive tubulointerstitial nephritis in a type 2 diabetes patient: a case report. CEN Case Rep. 2017 May;6(1):22-28. doi: 10.1007/s13730-016-0237-y. Epub 2016 Oct 03. PMID: 28509121; PMCID: PMC5438802.
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Methylprednisolone pulse therapy and intravenous cyclophosphamide therapy combined with cocktail therapy in severe pediatric Henoch-Schönlein purpura nephritis patient.

CEN case reports

Kanai H, Kobayashi A, Matsushita K, Sawanobori E, Sugita K, Higashida K.
PMID: 28509230
CEN Case Rep. 2013 May;2(1):117-122. doi: 10.1007/s13730-012-0056-8. Epub 2013 Jan 12.

Henoch-Schönlein purpura (HSP) is a common self-limited vasculitis in children. The long-term prognosis depends on renal involvement. In severe Henoch-Schönlein purpura nephritis (HSPN) patients, >50 % have crescent formation and nephrotic syndrome that are important predicted outcomes. Therefore, for...

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Kanai H, Kobayashi A, Matsushita K, et al. Methylprednisolone pulse therapy and intravenous cyclophosphamide therapy combined with cocktail therapy in severe pediatric Henoch-Schönlein purpura nephritis patient. CEN Case Rep. 2013;2(1):117-122doi: 10.1007/s13730-012-0056-8.
Kanai, H., Kobayashi, A., Matsushita, K., Sawanobori, E., Sugita, K., & Higashida, K. (2013). Methylprednisolone pulse therapy and intravenous cyclophosphamide therapy combined with cocktail therapy in severe pediatric Henoch-Schönlein purpura nephritis patient. CEN case reports, 2(1), 117-122. https://doi.org/10.1007/s13730-012-0056-8
Kanai, Hiroaki, et al. "Methylprednisolone pulse therapy and intravenous cyclophosphamide therapy combined with cocktail therapy in severe pediatric Henoch-Schönlein purpura nephritis patient." CEN case reports vol. 2,1 (2013): 117-122. doi: https://doi.org/10.1007/s13730-012-0056-8
Kanai H, Kobayashi A, Matsushita K, Sawanobori E, Sugita K, Higashida K. Methylprednisolone pulse therapy and intravenous cyclophosphamide therapy combined with cocktail therapy in severe pediatric Henoch-Schönlein purpura nephritis patient. CEN Case Rep. 2013 May;2(1):117-122. doi: 10.1007/s13730-012-0056-8. Epub 2013 Jan 12. PMID: 28509230; PMCID: PMC5411523.
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Membranous nephropathy associated with type 1 autoimmune pancreatitis and dominant glomerular IgG4 deposit.

CEN case reports

Sueta S, Kondo M, Matsubara T, Yasuhara Y, Akiyama S, Imai E, Amaike H, Tagawa M.
PMID: 28509238
CEN Case Rep. 2014 May;3(1):18-23. doi: 10.1007/s13730-013-0077-y. Epub 2013 May 03.

We report a case of membranous nephropathy associated with type 1 autoimmune pancreatitis. A 58-year-old man presented with anorexia. Work-up revealed a mass in the pancreatic head, which was subsequently resected. Pathological examination showed diffuse infiltration of immunoglobulin (Ig)...

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Sueta S, Kondo M, Matsubara T, et al. Membranous nephropathy associated with type 1 autoimmune pancreatitis and dominant glomerular IgG4 deposit. CEN Case Rep. 2013;3(1):18-23doi: 10.1007/s13730-013-0077-y.
Sueta, S., Kondo, M., Matsubara, T., Yasuhara, Y., Akiyama, S., Imai, E., Amaike, H., & Tagawa, M. (2014). Membranous nephropathy associated with type 1 autoimmune pancreatitis and dominant glomerular IgG4 deposit. CEN case reports, 3(1), 18-23. https://doi.org/10.1007/s13730-013-0077-y
Sueta, Shinichi, et al. "Membranous nephropathy associated with type 1 autoimmune pancreatitis and dominant glomerular IgG4 deposit." CEN case reports vol. 3,1 (2014): 18-23. doi: https://doi.org/10.1007/s13730-013-0077-y
Sueta S, Kondo M, Matsubara T, Yasuhara Y, Akiyama S, Imai E, Amaike H, Tagawa M. Membranous nephropathy associated with type 1 autoimmune pancreatitis and dominant glomerular IgG4 deposit. CEN Case Rep. 2014 May;3(1):18-23. doi: 10.1007/s13730-013-0077-y. Epub 2013 May 03. PMID: 28509238; PMCID: PMC5411534.
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Showing 1 to 12 of 2998 entries