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Korean Journal of Andrology

  to  Present  ISSN: 1229-1692

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Adenomatoid Tumor between the Epididymis and the Testis.

Young Hwan JI ; Sung Chan PARK ; Seung Kyu LEE ; Hyun Soo CHOO ; June KIM ; Hye Jeong CHOI ; Kyung Hyun MOON

Korean Journal of Andrology.2008;26(4):240-243.

Adenomatoid tumor is the most common paratesticular tumor with an anatomic distribution limited to the epididymis and it rarely invades to the tunica vaginalis, spermatic cord and ejaculatory duct. Adenomatoid tumor is a benign neoplasm that is thought to be of a mesothelial origin. The treatment of choice for adenomatoid tumor is local excision because of its benign nature and the absence of distant metastasis. We report here on a rare case of adenomatoid tumor that was found between the epididymis and the testis, and it was treated by local excision of tumor.
Adenomatoid Tumor ; Ejaculatory Ducts ; Epididymis ; Male ; Neoplasm Metastasis ; Spermatic Cord ; Testis

Adenomatoid Tumor ; Ejaculatory Ducts ; Epididymis ; Male ; Neoplasm Metastasis ; Spermatic Cord ; Testis

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Polycythemia as a Complication of Long-acting Injectable Testosterone Undecanoate.

Dong Sik SHIN ; Ki Won KO ; Sang Gan NAM ; Myeong Heon JIN ; Je Jong KIM ; Du Geon MOON

Korean Journal of Andrology.2008;26(4):237-239.

Polycythemia is a condition in which the red blood cell count is increased due to an inherited or acquired mutation, a physiologic response to hypoxia, autonomous erythropoietin production, or deliberate erythropoietin administration. Higher testosterone levels appear to act as a stimulus for erythropoiesis and testosterone replacement therapies have rarely been reported as causes of polycythemia. We report here a case of a 51-year-old man with polycythemia that was caused by long-acting testosterone undecanoate (Nebido(R)).
Anoxia ; Erythrocyte Count ; Erythropoiesis ; Erythropoietin ; Humans ; Middle Aged ; Polycythemia ; Testosterone

Anoxia ; Erythrocyte Count ; Erythropoiesis ; Erythropoietin ; Humans ; Middle Aged ; Polycythemia ; Testosterone

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A Case of Growth Hormone Deficiency that Induced Erectile Dysfunction.

Wan Shou CUI ; Young Jin KIM ; Hyung Jong NAM ; Yang Ho KANG ; Hong Koo HA ; Seong Ik BANG ; Hyun Jun PARK ; Nam Cheol PARK

Korean Journal of Andrology.2008;26(4):234-236.

Growth hormone deficiency is the medical condition of inadequate production of growth hormone. Growth hormone deficiency in adults is not common, but it may feature a diminished, lean body mass, poor bone density and a number of physical and psychological symptoms, including poor memory, social withdrawal and even depression. Abnormally low growth hormone levels in adults typically result in a diminished quality of life and it can even be disabling. The physical symptoms include loss of strength, stamina, and musculature. Growth hormone deficiency can also impair the biological and physiological/functional substrate of penile erection, which can be, at least in part, restored by the normalization of the plasma levels of growth hormone. This is a report on a 63-year-old man who suffered with severe erectile dysfunction and loss of libido due to growth hormone deficiency. Upon growth hormone administration, his erectile function improved dramatically.
Adult ; Bone Density ; Depression ; Erectile Dysfunction ; Growth Hormone ; Humans ; Libido ; Male ; Memory ; Middle Aged ; Penile Erection ; Plasma ; Quality of Life

Adult ; Bone Density ; Depression ; Erectile Dysfunction ; Growth Hormone ; Humans ; Libido ; Male ; Memory ; Middle Aged ; Penile Erection ; Plasma ; Quality of Life

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Clinical Efficacy and Safety of Long-acting Injectable Testosterone Undecanoate for Treating Patients with Testosterone Deficiency Syndrome.

Jae Hyun BAE ; Jeong Wu YU ; Je Jong KIM ; Du Geon MOON

Korean Journal of Andrology.2008;26(4):227-233.

PURPOSE: Long-acting injectable testosterone undecanoate (TU, Nebido(R)), a new parenteral testosterone preparation, has recently been introduced to avoid frequent injections of the conventional injectable esters. We performed this study to assess the efficacy and safety of long-acting injectable TU in patients who suffer with testosterone deficiency syndrome (TDS). MATERIALS AND METHODS: In this prospective, non-controlled single arm trial, a total of 33 patients (a mean age of 55.8+/-6.4 yrs) with TDS, as defined by serum testosterone levels of less than 3.5 ng/mL, were injected with 1000 mg of TU (4mL/ampule) on day 1, followed by another injection 6 weeks later with follow-up injections 3 months thereafter for a total of 54 weeks. Before and 18 and 54 weeks after the TU injections, the changes of the Aging Males' Symptoms (AMS) scale, the serum total testosterone, the lipid profiles, the CBC, the PSA level, the prostate volume by TRUS and the body mass index (BMI) were compared by Students' paired t-tests. Any adverse effects were also evaluated. RESULTS: Compared to the pretreatment results, the serum total testosterone level was significantly increased at 18 and 54 weeks (P<0.01), but there was no difference for the serum total testosterone level between weeks 18 and 54, that is, they were stable. The BMI was not significantly decreased at 54 weeks compared to pretreatment. Injectable TU also significantly improved the AMS scores, and especially in the sexual domain (P<0.01). The other data, except the hematocrit, was not significantly changed (P<0.05). Injectable TU did not show a harmful effect on the prostate during the 54 weeks. No patient reported any adverse side effects or events. CONCLUSIONS: Injectable TU effectively elevated the serum total testosterone levels and it maintained stable concentrations during the treatment period. Injectable TU significantly improved the total AMS score, but there were no reported significant changes in the body habitus and lipid profiles. Further large, well-controlled, long-term studies should be done to assess the effect of injectable TU on TDS patients.
Aging ; Arm ; Body Mass Index ; Esters ; Follow-Up Studies ; Hematocrit ; Humans ; Hypogonadism ; Prospective Studies ; Prostate ; Sorbitol ; Testosterone ; Tyramine

Aging ; Arm ; Body Mass Index ; Esters ; Follow-Up Studies ; Hematocrit ; Humans ; Hypogonadism ; Prospective Studies ; Prostate ; Sorbitol ; Testosterone ; Tyramine

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Patient Compliance and Associated Factors for Treatment with Alfuzosin XL 10mg (UroXatral(R)).

Tae Sung JUNG ; Yoon Dong KIM ; Myung Ho LEE ; Won Jae YANG ; Yun Seob SONG ; Young Ho PARK

Korean Journal of Andrology.2008;26(4):223-226.

PURPOSE: Alfuzosin XL (Sanofi-Aventis, UroXatral(R)) has to be taken just after a meal for the best efficacy due to its specific pharmacokinetics. We studied patient compliance and associated factors with regard to the correct instructions for taking alfuzosin XL. MATERIALS AND METHODS: Alfuzosin XL was prescribed to 62 patients from February to May 2008. At the first visit, we provided a prescription for alfuzosin XL with the instructions to "take one tablet just after dinner once a day". At the second visit, we evaluated patient compliance and the factors that influenced the patient compliance for taking the alfuzosin XL. The physician explained the instructions to the patients. At the third visit, we compared the compliance and associated factors with the results from the first visit. RESULTS: A total of 50 patients completed the study. After the first visit, twenty one patients (42.0%) were not taking the alfuzosin XL according to the prescription, that is, 20 patients took alfuzosin XL before going to bed, and one patient before meals. (p<0.05) After direct instructions by a physician, 49 patients (98.0%) took the alfuzosin XL correctly. (p<0.001) CONCLUSIONS: Taking alfuzosin XL as prescribed was accomplished in only 58% of patients. When alfuzosin XL is prescribed, the physicians should be aware of the importance of providing instructions directly to patients.
Compliance ; Humans ; Meals ; Patient Compliance ; Prescriptions ; Quinazolines

Compliance ; Humans ; Meals ; Patient Compliance ; Prescriptions ; Quinazolines

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Effect of IN-1130, a Novel Transforming Growth Factor-beta Type I Receptor Kinase (ALK5) Inhibitor, on a Rat Model of Peyronie's Disease Induced by Repeated Intratunical Injections of Fibrin.

Shuguang PIAO ; Munkhbayar TUMURBAATAR ; June Hyung OH ; Soo Hwan PARK ; Jun Kyu SUH ; Ji Kan RYU

Korean Journal of Andrology.2009;27(2):82-88.

PURPOSE: Transforming growth factor-beta1 (TGF-beta1) has been known to be involved in the pathogenesis of Peyronie's disease (PD). In the present study, we investigated the therapeutic effect of IN-1130, a novel small molecule inhibitor of activin receptor-like kinase (ALK)5, a type I receptor of TGF-beta, in an animal model of PD induced by fibrin. MATERIALS AND METHODS: Four-month-old male Sprague-Dawley rats were divided into three groups (n=4 per group): group 1, age-matched control; group 2, PD rats without treatment; group 3, PD rats receiving an intratunical injection of IN-1130 (on day 20, 5 mg/kg in 0.1 ml saline) into the lesion. PD was induced in rats through repeated injections of fibrin (50 microliter each of human fibrin and thrombin solutions, days 0, 3, and 6, respectively) into the tunica albuginea. Penile curvature was evaluated by use of an artificialerection test on day 30. The penis was then harvested and stained with Masson trichrome, hematoxylin- eosin, and antibody to vimentin and phospho-Smad2. RESULTS: PD rats receiving repeated intratunical injections of fibrin revealed an infiltration of inflammatory cells, including lymphocytes, plasma cells, and fibroblasts, and an increase in transnuclear expression of phospho-Smad2 in the fibrotic plaque. However, repeated intratunical injections of fibrin did not induce penile curvature. IN-1130 induced significant regression of fibrotic plaque through reduced infiltration of inflammatory cells and reduced transnuclear expression of phospho-Smad2. CONCLUSIONS: Inhibition of TGF-beta pathway through the use of ALK5 inhibitors may be a curative local treatment modality for PD.
Activin Receptors ; Animals ; Eosine Yellowish-(YS) ; Fibrin ; Fibroblasts ; Humans ; Imidazoles ; Lymphocytes ; Male ; Models, Animal ; Penile Induration ; Penis ; Phosphotransferases ; Plasma Cells ; Quinoxalines ; Rats ; Rats, Sprague-Dawley ; Thrombin ; Transforming Growth Factor beta ; Vimentin

Activin Receptors ; Animals ; Eosine Yellowish-(YS) ; Fibrin ; Fibroblasts ; Humans ; Imidazoles ; Lymphocytes ; Male ; Models, Animal ; Penile Induration ; Penis ; Phosphotransferases ; Plasma Cells ; Quinoxalines ; Rats ; Rats, Sprague-Dawley ; Thrombin ; Transforming Growth Factor beta ; Vimentin

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Penile Rehabilitation.

Dae Yul YANG

Korean Journal of Andrology.2009;27(2):74-81.

Erectile dysfunction following radical prostatectomy is significant quality of life issue even with increased understanding of the anatomy and advancement of surgical skills such as nerve sparing prostatectomy, laproscopic, and robotic surgery. The changes of neuropraxia, ischemic and hypoxic injury vascular damage, fibrotic remodeling, and venous leak are all believed to contribute to erectile dysfunction. Penile rehabilitation is the use of any drug or device at or after radical prostatectomy to preserving penile function and earlier return of potency. There are no generally accepted guidelines for penile rehabilitation regiments. There exist several popular options such as PDE5I (phosphodiesterase type 5 inhibitor), intracorporeal injection of vasoactive agent, vacuum device, intraurethral alprostadil, and combination of these modalities. Current animal and human data support the primary use of PDE5I (phosphodiesterase type 5 inhibitor) for nerve sparing and injection of vasoactive agent for supposed nerve injury patients. Some experimental modalities including hyperbaric oxygen therapy, neuromodulator, and stem cell strategies are under preclinical study. This paper will review the literatures involving both basic and clincial evidences for rehabilitation approaches following radical prostatectomy.
Alprostadil ; Animals ; Erectile Dysfunction ; Humans ; Hyperbaric Oxygenation ; Male ; Neurotransmitter Agents ; Prostatectomy ; Quality of Life ; Stem Cells ; Vacuum

Alprostadil ; Animals ; Erectile Dysfunction ; Humans ; Hyperbaric Oxygenation ; Male ; Neurotransmitter Agents ; Prostatectomy ; Quality of Life ; Stem Cells ; Vacuum

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A Manual of 2008 ISA, ISSAM, EAU, EAA and ASA Recommendations: Investigation, Treatment and Monitoring of Late-onset Hypogonadism in Males.

Nam Cheol PARK

Korean Journal of Andrology.2009;27(2):63-73.

The 2008 new recommendations from professional societies including ISA, ISSAM, EAU, EAA and ASA on the investigation, treatment and monitoring of late-onset hypogonadism in males provide updated evidence-based informations for clinicians who diagnose and treat patients with adult-onset, age-associated testosterone deficiency
Humans ; Hypogonadism ; Male ; Testosterone

Humans ; Hypogonadism ; Male ; Testosterone

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A Case of Neurogenic Bladder and Erectile Dysfunction due to Decompression Sickness.

Han Seok KIM ; Du Yong KIM ; Byeong Ju SEONG ; Seong Ju KIM ; Jae Min CHUNG ; Seong CHOI

Korean Journal of Andrology.2006;24(1):51-53.

Decompression sickness is a disease caused by nitrogen bubbles in the tissues of divers who move too rapidly from environments of higher to those of lower atmospheric pressures. Nitrogen breathed in air under pressure dissolves in tissue fluids. When ambient pressure is reduced too rapidly, nitrogen goes out of solution faster than it can be circulated to the lungs for expiration. Gaseous nitrogen then accumulates in the joint spaces and peripheral circulation, impairing tissue oxygenation. We report a case of patient who experiencedneurogenic bladder and erectile dysfunction after decompression sickness. To our knowledge, this is the first case of neurogenic bladder and erectile dysfunction due to decompression sickness in the Korean literature.
Atmospheric Pressure ; Decompression Sickness* ; Decompression* ; Erectile Dysfunction* ; Humans ; Joints ; Lung ; Male ; Nitrogen ; Oxygen ; Urinary Bladder ; Urinary Bladder, Neurogenic*

Atmospheric Pressure ; Decompression Sickness* ; Decompression* ; Erectile Dysfunction* ; Humans ; Joints ; Lung ; Male ; Nitrogen ; Oxygen ; Urinary Bladder ; Urinary Bladder, Neurogenic*

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Effect of Metformin on the Expression of Nitric Oxide Synthase in High Fat Fed Obese Rats.

Chang Jun YOON ; Woo Sung JEON ; Yong Woon KIM ; Ki Hak MOON

Korean Journal of Andrology.2006;24(1):44-50.

PURPOSE: Obesity is a well known risk factorfor erectile dysfunction, and metformin normalizes androgen levels in patients with polycystic ovary syndrome and decreases body fat and leptin concentration in normal weight men. Thus, we hypothesized that metformin may restore the neuroendocrine abnormalities associated with obesity and improve erectile dysfunction. MATERIALS AND METHODS: Obesity was induced by a high fat(HF) diet fed for 4 months, and then metformin(300 mg/kg/day) was administered for 4 weeks. Penile nitric oxide synthase(NOS) expression and luteinizing hormone (LH), follicle stimulating hormone(FSH), testosterone, leptin, corticotropin releasing factor(CRF), adrenocorticotropin (ACTH), and proopiomelanocortin(POMC) were evaluated in control and HF obese rats. RESULTS: Penile nNOS and eNOS were suppressed markedly, and serum leptin and FSH were increased in HF rats compared to controls. However, POMCexpression in the hypothalamus was decreased in HF rats compared to controls,despite slightly elevated cerebrospinal fluid(CSF) leptin concentration. Metformin treatment for 4 weeks restored penile nNOS and eNOS expression, decreased serum leptin, increased POMC expression in the hypothalamus, and decreased serum concentration of FSH and CRF in HF rats. Surprisingly, metformin increased CSF leptin concentration in both control and HF rats. CONCLUSIONS: These results suggested that NOS expression was suppressed by the HF diet, but restored by metformin treatment. The effect of metformin on NOS expression resulted from not only a leptin sensitizing effect but also through a normalizing effect on levels of endocrine factors.
Adipose Tissue ; Adrenocorticotropic Hormone ; Animals ; Diet ; Erectile Dysfunction ; Humans ; Hypothalamus ; Leptin ; Luteinizing Hormone ; Male ; Metformin* ; Nitric Oxide Synthase* ; Nitric Oxide* ; Obesity ; Polycystic Ovary Syndrome ; Pro-Opiomelanocortin ; Rats* ; Testosterone

Adipose Tissue ; Adrenocorticotropic Hormone ; Animals ; Diet ; Erectile Dysfunction ; Humans ; Hypothalamus ; Leptin ; Luteinizing Hormone ; Male ; Metformin* ; Nitric Oxide Synthase* ; Nitric Oxide* ; Obesity ; Polycystic Ovary Syndrome ; Pro-Opiomelanocortin ; Rats* ; Testosterone

Country

Republic of Korea

Publisher

Korean Society for Sexual Medicine and Andrology

ElectronicLinks

http://wjmh.org/

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E-mail

Abbreviation

Korean J Androl

Vernacular Journal Title

대한남성과학회지

ISSN

1229-1692

EISSN

Year Approved

2007

Current Indexing Status

Currently Indexed

Start Year

Description

Current Title

The World Journal of Men's Health

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