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Journal articles on the topic 'CD4 lymphocytopenia'

Author: Grafiati
Published: 4 June 2025
Last updated: 23 June 2025

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1

Brooks, Joel P., and Gisoo Ghaffari. "Idiopathic CD4 lymphocytopenia." Allergy and Asthma Proceedings 37, no. 6 (2016): 501–4. http://dx.doi.org/10.2500/aap.2016.37.3992.

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2

Régent, Alexis, Brigitte Autran, Guislaine Carcelain, et al. "Idiopathic CD4 Lymphocytopenia." Medicine 93, no. 2 (2014): 61–72. http://dx.doi.org/10.1097/md.0000000000000017.

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3

Walker, Ulrich A., and Klaus Warnatz. "Idiopathic CD4 lymphocytopenia." Current Opinion in Rheumatology 18, no. 4 (2006): 389–95. http://dx.doi.org/10.1097/01.bor.0000231908.57913.2f.

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4

Yarmohammadi, Hale, and Charlotte Cunningham-Rundles. "Idiopathic CD4 lymphocytopenia." Annals of Allergy, Asthma & Immunology 119, no. 4 (2017): 374–78. http://dx.doi.org/10.1016/j.anai.2017.07.021.

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5

Freier, S., E. Kerem, Z. Dranitzki, et al. "Hereditary CD4+ T lymphocytopenia." Archives of Disease in Childhood 78, no. 4 (1998): 371–72. http://dx.doi.org/10.1136/adc.78.4.371.

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6

DeHovitz, Jack A., Joseph Feldman, and Sheldon Landesman. "Idiopathic CD4+ T-Lymphocytopenia." New England Journal of Medicine 329, no. 14 (1993): 1045–46. http://dx.doi.org/10.1056/nejm199309303291418.

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7

Cardoso, António, João Gouveia, Claudia Viegas, Fernanda Martins, Carlos Maltez, and Fátima Campante. "P0726 IDIOPATHIC CD4 LYMPHOCYTOPENIA." European Journal of Internal Medicine 20 (May 2009): S237. http://dx.doi.org/10.1016/s0953-6205(09)60745-7.

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8

Dunn, David, and Marie-Louise Newell. "IDIOPATHIC CD4+ T LYMPHOCYTOPENIA." Pediatric Infectious Disease Journal 12, no. 8 (1993): 705. http://dx.doi.org/10.1097/00006454-199308000-00024.

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9

Soriano, V., I. Hewlett, A. Heredia, et al. "Idiopathic CD4+ T-lymphocytopenia." Lancet 340, no. 8819 (1992): 607–9. http://dx.doi.org/10.1016/0140-6736(92)92140-b.

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10

TORIKAI, Katsutaka. "Idiopathic CD4+ T-Lymphocytopenia." Internal Medicine 36, no. 11 (1997): 759. http://dx.doi.org/10.2169/internalmedicine.36.759.

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11

Vijayakumar, Saravanakumari, Stalin Viswanathan, and Rajeswari Aghoram. "Idiopathic CD4 Lymphocytopenia: Current Insights." ImmunoTargets and Therapy Volume 9 (May 2020): 79–93. http://dx.doi.org/10.2147/itt.s214139.

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12

Zonios, Dimitrios I., Judith Falloon, Chiung-Yu Huang, Doreen Chaitt, and John E. Bennett. "Cryptococcosis and Idiopathic CD4 Lymphocytopenia." Medicine 86, no. 2 (2007): 78–92. http://dx.doi.org/10.1097/md.0b013e31803b52f5.

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13

LOBATO, MARK N., THOMAS J. SPIRA, and MARTHA F. ROGERS. "CD4+ T lymphocytopenia in children." Pediatric Infectious Disease Journal 14, no. 6 (1995): 527–35. http://dx.doi.org/10.1097/00006454-199506000-00011.

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14

Cheung, Loretta, and Miriam Weinstein. "Idiopathic CD4 T-Cell Lymphocytopenia." Journal of Cutaneous Medicine and Surgery 20, no. 5 (2016): 470–73. http://dx.doi.org/10.1177/1203475416638045.

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Importance: Idiopathic CD4 T-cell lymphocytopenia (ICL) is an immunodeficiency disorder that presents with a decrease in CD4+ T cells without evidence of a human immunodeficiency virus infection. It is most commonly diagnosed after a patient presents with an opportunistic infection and can also be associated with malignancies and autoimmune diseases. This case presentation and literature review highlights the common skin findings in patients with ICL, mainly recalcitrant warts, and discusses the treatment options available. Observations: The patient described is the youngest reported with ICL presenting with isolated cutaneous findings of recalcitrant warts and psoriasis. Many treatment options were tried for the warts, with the most significant response to acitretin. Conclusions and Relevance: This case highlights the importance of considering underlying immunodeficiency in patients with recalcitrant warts as well as developing treatment plans. Such patients require close follow-up by both dermatology and immunology to monitor for the development of other diseases related to ICL.
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15

Mukherjee, Aparna, Rakesh Lodha, and S. K. Kabra. "Idiopathic CD4+ T-cell lymphocytopenia." Indian Journal of Pediatrics 76, no. 4 (2009): 430–32. http://dx.doi.org/10.1007/s12098-009-0002-8.

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16

Siderits, Richard H., Osman Ouattara, Alan Marcus, Hong Guang Gao, Hong Bing Deng, and Janusz Godyn. "Case study documenting the diagnosis of idiopathic CD4+ Lymphocytopenia in a patient with atypical fungal infection (disseminated blastomycosis) by FNA of adrenal mass." CytoJournal 7 (August 5, 2010): 13. http://dx.doi.org/10.4103/1742-6413.67106.

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Idiopathic CD4+ lymphocytopenia, described in 1992 by the Centers for Disease Control, is characterized by persistent CD4+ lymphocytopenia (less than 300 cells per micro-liter) in nonimmunosuppressed, HIV negative individuals, who present with atypical infections. This rare though likely undiagnosed entity is associated with chronic disseminated forms of either fungal or bacterial infections in otherwise healthy adults. We report a case of a 59-year-old male with ring-enhancing brain lesions, bilateral adrenal masses, lung and vocal cord nodules, where the diagnosis of exclusion was metastatic malignancy. Fine needle aspiration (FNA) of the adrenal mass and a subsequent vocal cord biopsy confirmed chronic widely disseminated blastomycosis. Flow cytometric evaluation of peripheral blood documented persistent selective CD4+ lymphocytopenia with T8 (suppressor) T-Lymphocyte count within normal range. We believe that idiopathic CD4+ lymphocytopenia is an important etiologic factor to be considered for patients who present with mass lesions and are diagnosed by FNA with atypical fungal infections. We relate the diagnostic criteria for idiopathic CD4+ lymphocytopenia and the importance of providing on-site triage for FNA samples for fungal studies and correlation for flow cytometry.
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17

Chen, Bing, Chaoyang Guan, Peipei Xu, Xiaoyan Shao, Rong-Fu Zhou, and Jian Ouyang. "Idiopathic CD4+ T-Lymphocytopenia — One Case Report from China." Blood 124, no. 21 (2014): 4969. http://dx.doi.org/10.1182/blood.v124.21.4969.4969.

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Abstract The patient was a 55-year-old femal staff who presented with gingivitis in July 2009. The result of blood routine test indicated WBC was 2.6×109/L, neutrophil count was 0, lymphocyte count was 2.1×109/L, hemoglobin count was 119g/L, and PLT count was 342×109/L. In addition, the ratio of heterotype lymphocytes was 8% in blood smear. Lymphocyte subsets analysis showed that CD3+T lymphocytes took up 57%, CD3+ CD4+ T lymphocytes took up 12% (count 250 per cubic millimeter), CD3+ CD8+ T lymphocytes accounted for 40% (count 840 per cubic millimeter), NK cells took up 40% and the ratio of CD4/CD8 and CD4/CD3 were 0.3 and 0.21 respectively. The patient’s liver function was abnormal and serological testing of HIV, EBV and CMV was negative. Enterobacter cloacae was cultured from the secretions of gum. Bone marrow smear showed active proliferation of cells with lymphocytes took up 32% which consisted of T cells with normal morphology mainly. The chromosome of the patient was normal. Ultrasound test showed enlargement of the lymph nodes in the neck with normal echo. She responded well to treatment with antibiotics, granulocyte colony-stimulating factor and supportive care. In September 2009, her CD4+T lymphocyte count was still very low (440 per cubic millimeter) and the ratio of CD4+ /CD3+ lymphocytes was 0.28. Then she started intramuscular injection of thymopentin 1mg daily for one month and decreased the frequency from twice or three times a week to once every ten days. She occasionally felt swelling pain of her gum and lymph nodes. CD4+ T lymphocyte count was 500~900 per cubic millimeter and CD8+ T lymphocyte was 800~1400 per cubic millimeter. In the Junes of 2010 and 2013, her ratio of CD4/CD3 unprovoked declined (to 0.17) with mild hepatic dysfunction. After increasing the injection frequency of Thymosin α1,her CD4+lymphocyte count increased (less than 740 per cubic millimeter). She is asymptomatic at this writing. During the course, gene rearrangement of TCRγ-VJ1and TCRγVJ2 was positive in June 2010 and turned negative in June 2013. Results of bone marrow smear and biopsy were normal and multiple serologic testing of HIV, EBV and CMV was negative. Her auto-antibodies were tested negative too. A PET-CT scan found small lymph nodes on both sides of her neck with average SUV value of 2.3 in June, 2013. She was not homosexual. She had constipation for many years while endoscopy of the stomach and intestine was normal. She had no history of taking immune-suppressive drugs or blood transfusion except for hysteromyomectomy in 2002. She had no special family history. According to the American CDC’s diagnostic criteria in 1992, this patient was diagnosed with idiopathic CD4+ T-lymphocytopenia. The disease is extremely rare, only two cases reported so far in China. Doctors in the clinical work in patients with recurrent infections especially opportunistic infections should do routine lymphocyte immune classification which can improve the diagnostic rate of this disease. The prognosis of the disease is mostly good. Thymopentin or thymosin may improve the degree of immune deficiency and reduce infections. Disclosures No relevant conflicts of interest to declare.
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18

Ozarmagan, G., EZ Ozgüroglu, MU Maden, and S. Oztürk. "Refractory ulcerative lupus vulgaris associated with CD4 lymphocytopenia, inversion of chromosome 14, primary amenorrhoea and mental retardation." Acta Dermato-Venereologica 77, no. 4 (1997): 309–10. http://dx.doi.org/10.2340/0001555577309310.

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A case of ulcerative lupus vulgaris, confirmed by polymerase chain reaction (PCR) is reported. The initial lesion of our case was a papule on the nose, which progressed during antituberculous treatment and caused cartilage destruction and ectropion. Immunological analysis revealed CD4 lymphocytopenia, and the possibility of idiopathic CD4 lymphocyte deficiency was considered. In addition, the patient had primary amenorrhoea, mental retardation and inversion of chromosome 14. CD4 lymphocytopenia and chromosomal abnormality are the possible causes of antituberculous treatment failure.
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19

Rapisarda, Francesco, Luca Zanoli, Grazia Portale, Salvo Scuto, and Pietro Castellino. "A Case Report of an Atypical Presentation of IgG4-Related Disease and Idiopathic CD4 Lymphocytopenia." Case Reports in Medicine 2015 (2015): 1–5. http://dx.doi.org/10.1155/2015/512370.

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The IgG4-related disease is a fibroinflammatory disease characterized by tumefactive lesions, a dense lymphoplasmacytic infiltrate rich in IgG4-positive plasma cells, storiform fibrosis, and, often but not always, elevated serum levels of IgG4. Idiopathic CD4 lymphocytopenia is a heterogenic and rare syndrome characterized by the detection of a persistent absolute CD4 T cells count <300 cells/mm3(or <20% of total T cells) in more than one occasion and no evidence of HIV infection in absence of immunodeficiency or therapy associated with depressed levels of CD4 T cells. We report the case of a 50-year-old man with a multiorgan IgG4-related disease presenting in a temporal association with a profound and symptomatic idiopathic CD4 lymphocytopenia. Both clinical pictures improved after steroid treatment. Idiopathic CD4 lymphocytopenia has been associated with a number of autoimmune conditions but, to the best of our knowledge, this is the first case in which an association with the IgG4-related disease is reported.
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20

Jha, Sanjeev, Parasar Ghosh, and Vikas Agarwal. "Cryptococcal meningitis unmasking idiopathic CD4 lymphocytopenia." Neurology India 55, no. 3 (2007): 312. http://dx.doi.org/10.4103/0028-3886.35700.

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21

Ete, Tony, Sumantro Mondal, Debanjali Sinha, et al. "Idiopathic CD4 lymphocytopenia with adrenal histoplasmosis." International Journal of Medical Science and Public Health 3, no. 12 (2014): 1562. http://dx.doi.org/10.5455/ijmsph.2014.170920144.

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22

Puri, Vinod, AshishKumar Duggal, and Neera Chaudhry. "Idiopathic CD4 lymphocytopenia with sensorimotor polyneuropathy." Annals of Indian Academy of Neurology 19, no. 3 (2016): 381. http://dx.doi.org/10.4103/0972-2327.165470.

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23

HARDMAN, C. M., B. S. BAKER, J. LORTAN, et al. "Active psoriasis and profound CD4+ lymphocytopenia." British Journal of Dermatology 136, no. 6 (1997): 930–32. http://dx.doi.org/10.1046/j.1365-2133.1997.01802.x.

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24

HARDMAN, C. M., B. S. BAKER, J. LORTAN, et al. "Active psoriasis and profound CD4+lymphocytopenia." British Journal of Dermatology 136, no. 6 (1997): 930–32. http://dx.doi.org/10.1111/j.1365-2133.1997.tb03936.x.

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25

BORDIN, G., M. BALLARE, S. PAGLINO, et al. "Idiopathic CD4+ lymphocytopenia and systemic vasculitis." Journal of Internal Medicine 240, no. 1 (1996): 37–41. http://dx.doi.org/10.1046/j.1365-2796.1996.447785000.x.

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26

Stetson, Cloyce L., Ronald P. Rapini, Stephen K. Tyring, and Robert C. Kimbrough. "CD4+ T lymphocytopenia with disseminated HPV." Journal of Cutaneous Pathology 29, no. 8 (2002): 502–5. http://dx.doi.org/10.1034/j.1600-0560.2002.290809.x.

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27

Gupta, Dhananjay, Anish Mehta, Nikith Shetty, et al. "Idiopathic CD4 lymphocytopenia in neurological disorders." Clinical Neurology and Neurosurgery 195 (August 2020): 105923. http://dx.doi.org/10.1016/j.clineuro.2020.105923.

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28

Calderón, E., B. Sánchez, F. J. Medrano, P. Stiefel, and M. Leal. "CD4+ T-lymphocytopenia in the elderly." European Journal of Clinical Microbiology & Infectious Diseases 14, no. 1 (1995): 75–77. http://dx.doi.org/10.1007/bf02112629.

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29

Wladis, Edward J. "Idiopathic CD4+ Lymphocytopenia and Sjogren Syndrome." Archives of Ophthalmology 123, no. 7 (2005): 1012. http://dx.doi.org/10.1001/archopht.123.7.1012-a.

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30

Tadjali, Armand, Sharon Pan, Elias Perli, and Toni Keaton. "Clinical presentation of idiopathic CD4 lymphocytopenia." BMJ Case Reports 16, no. 7 (2023): e254746. http://dx.doi.org/10.1136/bcr-2023-254746.

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An otherwise healthy man (60s) presented to our emergency department 5 years ago with stroke-like symptoms. Underlying cryptococcal meningitis infection was ultimately discovered leading to extensive workup to rule out underlying malignancy and HIV infection. Results returned negative with the exception of a CD4 count less than 25 /mm3. Several years later, he again presented to the emergency department with fatigue. He was then found to have severe anaemia with underlyingMycobacterium aviumcomplex (MAC) infection involving the bone marrow and a left psoas abscess. After multiple courses of antibiotic therapy targeted towards MAC, the infection persisted due to bone marrow involvement. By diagnosis of exclusion, he was eventually found to have idiopathic CD4 lymphocytopenia. Here we describe this condition, which has the potential to cause significant morbidity, and obligates the need for high clinical suspicion for timely diagnosis to enhance life quality and outcomes for patients.
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31

Grimfors, G., G. Holm, H. Mellstedt, PO Schnell, O. Tullgren, and M. Bjorkholm. "Increased blood clearance rate of indium-111 oxine-labeled autologous CD4+ blood cells in untreated patients with Hodgkin's disease." Blood 76, no. 3 (1990): 583–89. http://dx.doi.org/10.1182/blood.v76.3.583.583.

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Abstract Untreated patients with Hodgkin's disease (HD) have a blood T- lymphocytopenia mainly caused by a reduction of the CD4+ subset. Indirect support for a sequestration of T cells in the spleen and tumor- involved lymphoid tissue has accumulated. To test the hypothesis that the blood CD4 T-lymphocytopenia in patients with HD is caused by an altered lymphocyte traffic, 12 untreated HD patients and five in complete clinical remission (CCR) were studied. Blood lymphocytes were collected by leukapheresis and gradient centrifugation, and were further purified by an adherence step. The cells were labeled with indium-111 oxine and reinfused intravenously into the patient. The radioactivity of CD4+ and CD8+ blood lymphocytes separated by immunoabsorption was measured from serial blood samples. CD4+ cells were eliminated more rapidly in untreated patients than patients in CCR. Repeated gamma camera imaging after autotransfusion of indium-111 oxine labeled cells demonstrated an accumulation of radioactivity in tumor-involved tissue of untreated patients. These findings support the concept of an enhanced elimination of CD4+ cells in patients with active HD that may contribute to the observed blood T-lymphocytopenia and may reflect a biologic response to the tumor.
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32

Grimfors, G., G. Holm, H. Mellstedt, PO Schnell, O. Tullgren, and M. Bjorkholm. "Increased blood clearance rate of indium-111 oxine-labeled autologous CD4+ blood cells in untreated patients with Hodgkin's disease." Blood 76, no. 3 (1990): 583–89. http://dx.doi.org/10.1182/blood.v76.3.583.bloodjournal763583.

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Untreated patients with Hodgkin's disease (HD) have a blood T- lymphocytopenia mainly caused by a reduction of the CD4+ subset. Indirect support for a sequestration of T cells in the spleen and tumor- involved lymphoid tissue has accumulated. To test the hypothesis that the blood CD4 T-lymphocytopenia in patients with HD is caused by an altered lymphocyte traffic, 12 untreated HD patients and five in complete clinical remission (CCR) were studied. Blood lymphocytes were collected by leukapheresis and gradient centrifugation, and were further purified by an adherence step. The cells were labeled with indium-111 oxine and reinfused intravenously into the patient. The radioactivity of CD4+ and CD8+ blood lymphocytes separated by immunoabsorption was measured from serial blood samples. CD4+ cells were eliminated more rapidly in untreated patients than patients in CCR. Repeated gamma camera imaging after autotransfusion of indium-111 oxine labeled cells demonstrated an accumulation of radioactivity in tumor-involved tissue of untreated patients. These findings support the concept of an enhanced elimination of CD4+ cells in patients with active HD that may contribute to the observed blood T-lymphocytopenia and may reflect a biologic response to the tumor.
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33

Yogarajah, Meera, and Bhradeev Sivasambu. "Kikuchi-Fujimoto Disease Associated with Symptomatic CD4 Lymphocytopenia." Case Reports in Rheumatology 2014 (2014): 1–3. http://dx.doi.org/10.1155/2014/768321.

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Kikuchi-Fujimoto disease is a rare benign condition of necrotising histiocytic lymphadenitis with unknown aetiology. We describe here a 30-year-old African American female who presented with fever, generalized rash, cervical lymphadenopathy, and oral candidiasis and was found to have Kikuchi-Fujimoto disease on lymph node biopsy with low CD4 count. The initial presentation was concerning for acute retroviral infection. Her HIV serology and HIV RNA PCR were negative however she had low CD4 count with reversal of CD4/CD8 ratio. Although low CD4 count has been associated with autoimmune disease, it has not been described with Kikuchi-Fujimoto disease. We report the first case of Kikuchi-Fujimoto disease associated with symptomatic CD4 lymphocytopenia.
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34

Hingolikar, AnkitaPrashant, PreetMukesh Shah, Shruti Tandan, and VijayWaman Dhakre. "Idiopathic CD4 lymphocytopenia presenting as cryptococcal meningitis." Journal of Global Infectious Diseases 13, no. 1 (2021): 56. http://dx.doi.org/10.4103/jgid.jgid_182_20.

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35

Lin, Syh-Jae, Hsun-Chin Chao, Dah-Chin Yan, and Ming-Ling Kuo. "IDIOPATHIC CD4+T LYMPHOCYTOPENIA IN TWO SIBLINGS." Pediatric Hematology and Oncology 18, no. 2 (2001): 153–56. http://dx.doi.org/10.1080/088800101300003008.

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36

Ish, Pranav, Harpreet Singh, S. Anuradha, and Richa Dewan. "Idiopathic CD4 lymphocytopenia presenting as cryptococcal meningitis." Astrocyte 2, no. 1 (2015): 38. http://dx.doi.org/10.4103/2349-0977.168253.

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37

De Socio, Giuseppe V. L., Roberto Gerli, and Francesco Menichetti. "Disseminated tuberculosis and idiopathic CD4+ T-lymphocytopenia." Clinical Microbiology and Infection 5, no. 10 (1999): 653–54. http://dx.doi.org/10.1111/j.1469-0691.1999.tb00426.x.

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38

Guma, Michael. "Letters: CD4+ Lymphocytopenia in Systemic Lupus Erythematosus." Annals of Internal Medicine 120, no. 2 (1994): 168. http://dx.doi.org/10.7326/0003-4819-120-2-199401150-00022.

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39

Laurence, Jeffrey. "Letters: CD4+ Lymphocytopenia in Systemic Lupus Erythematosus." Annals of Internal Medicine 120, no. 2 (1994): 168. http://dx.doi.org/10.7326/0003-4819-120-2-199401150-00023.

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40

Aghoram, Rajeswari, and Sunil K. Narayan. "Progressive multifocal leukoencephalopathy in idiopathic CD4+ lymphocytopenia." Journal of NeuroVirology 24, no. 4 (2018): 526–28. http://dx.doi.org/10.1007/s13365-018-0638-0.

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41

Reichert, T. A. "Idiopathic CD4+ T-lymphocytopenia: a quantitative view." Lancet 341, no. 8845 (1993): 636. http://dx.doi.org/10.1016/0140-6736(93)90402-3.

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42

Delgado-Alvarado, Manuel, María José Sedano, Vicente González-Quintanilla, Enrique Marco de Lucas, José Miguel Polo, and José Berciano. "Progressive multifocal leukoencephalopathy and idiopathic CD4 lymphocytopenia." Journal of the Neurological Sciences 327, no. 1-2 (2013): 75–79. http://dx.doi.org/10.1016/j.jns.2013.02.002.

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43

HAYASHI, Toshiaki, Yuji HINODA, Tohru TAKAHASHI, et al. "Idiopathic CD4+ T-Lymphocytopenia with Bowen's Disease." Internal Medicine 36, no. 11 (1997): 822–24. http://dx.doi.org/10.2169/internalmedicine.36.822.

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44

Umamaheshwari, S., S. Gopal, MN Sumana, and MS Shetty. "Idiopathic CD4+ T lymphocytopenia: A case report." Journal of Postgraduate Medicine 66, no. 2 (2020): 102. http://dx.doi.org/10.4103/jpgm.jpgm_324_19.

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45

Damara, FA, and AN Ramdhani. "Idiopathic CD4+T lymphocytopenia: A case report." Journal of Postgraduate Medicine 66, no. 4 (2020): 226. http://dx.doi.org/10.4103/jpgm.jpgm_718_20.

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46

&NA;. "CD4+ lymphocytopenia in HIV-seronegative homosexual men." AIDS 7, no. 9 (1993): 1271–73. http://dx.doi.org/10.1097/00002030-199309000-00022.

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47

Stasi, R., G. Delpoeta, A. Venditti, U. Coppetelli, M. Masi, and G. Papa. "Clinical heterogeneity of idiopathic CD4 + T lymphocytopenia." Journal of Internal Medicine 235, no. 1 (1994): 92–93. http://dx.doi.org/10.1111/j.1365-2796.1994.tb01039.x.

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48

de Paula Motta Rubini, Norma, Albertina Varandas Capelo, Eliane Miranda da Silva, et al. "Idiopathic CD4 Lymphocytopenia: Clinical and Immunological Aspects." Journal of Allergy and Clinical Immunology 131, no. 2 (2013): AB70. http://dx.doi.org/10.1016/j.jaci.2012.12.913.

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49

Leiding, J. W., J. Heimall, Y. Song, S. M. Holland, R. M. Siegel, and A. F. Freeman. "Idiopathic CD4+ Lymphocytopenia: Clinical and Autoimmune Phenotype." Journal of Allergy and Clinical Immunology 127, no. 2 (2011): AB89. http://dx.doi.org/10.1016/j.jaci.2010.12.358.

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50

Pasic, Srdjan, Predrag Minic, Slobodan Dzudovic, Aleksandra Minic, and Bojana Slavkovic. "Idiopathic CD4+ lymphocytopenia and juvenile laryngeal papillomatosis." Pediatric Pulmonology 39, no. 3 (2005): 281–83. http://dx.doi.org/10.1002/ppul.20173.

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