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Article ; Online: The role of NADPH oxidases in infectious and inflammatory diseases.

Taylor, Jared P / Tse, Hubert M

2021 Volume 48, Page(s) 102159

Abstract: Nicotinamide adenine dinucleotide phosphate (NADPH) oxidases (NOX) are enzymes that generate superoxide or hydrogen peroxide from molecular oxygen utilizing NADPH as an electron donor. There are seven enzymes in the NOX family: NOX1-5 and dual oxidase ( ... ...

Abstract	Nicotinamide adenine dinucleotide phosphate (NADPH) oxidases (NOX) are enzymes that generate superoxide or hydrogen peroxide from molecular oxygen utilizing NADPH as an electron donor. There are seven enzymes in the NOX family: NOX1-5 and dual oxidase (DUOX) 1-2. NOX enzymes in humans play important roles in diverse biological functions and vary in expression from tissue to tissue. Importantly, NOX2 is involved in regulating many aspects of innate and adaptive immunity, including regulation of type I interferons, the inflammasome, phagocytosis, antigen processing and presentation, and cell signaling. DUOX1 and DUOX2 play important roles in innate immune defenses at epithelial barriers. This review discusses the role of NOX enzymes in normal physiological processes as well as in disease. NOX enzymes are important in autoimmune diseases like type 1 diabetes and have also been implicated in acute lung injury caused by infection with SARS-CoV-2. Targeting NOX enzymes directly or through scavenging free radicals may be useful therapies for autoimmunity and acute lung injury where oxidative stress contributes to pathology.
MeSH term(s)	COVID-19 ; Dual Oxidases ; Humans ; NADPH Oxidases/genetics ; Reactive Oxygen Species ; SARS-CoV-2
Chemical Substances	Reactive Oxygen Species ; Dual Oxidases (EC 1.11.1.-) ; NADPH Oxidases (EC 1.6.3.-)
Language	English
Publishing date	2021-10-04
Publishing country	Netherlands
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Review
ZDB-ID	2701011-9
ISSN	2213-2317 ; 2213-2317
ISSN (online)	2213-2317
ISSN	2213-2317
DOI	10.1016/j.redox.2021.102159
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Article ; Online: The role of NADPH oxidases in infectious and inflammatory diseases

Jared P. Taylor / Hubert M. Tse

Redox Biology, Vol 48, Iss , Pp 102159- (2021)

2021

Abstract	Nicotinamide adenine dinucleotide phosphate (NADPH) oxidases (NOX) are enzymes that generate superoxide or hydrogen peroxide from molecular oxygen utilizing NADPH as an electron donor. There are seven enzymes in the NOX family: NOX1-5 and dual oxidase (DUOX) 1–2. NOX enzymes in humans play important roles in diverse biological functions and vary in expression from tissue to tissue. Importantly, NOX2 is involved in regulating many aspects of innate and adaptive immunity, including regulation of type I interferons, the inflammasome, phagocytosis, antigen processing and presentation, and cell signaling. DUOX1 and DUOX2 play important roles in innate immune defenses at epithelial barriers. This review discusses the role of NOX enzymes in normal physiological processes as well as in disease. NOX enzymes are important in autoimmune diseases like type 1 diabetes and have also been implicated in acute lung injury caused by infection with SARS-CoV-2. Targeting NOX enzymes directly or through scavenging free radicals may be useful therapies for autoimmunity and acute lung injury where oxidative stress contributes to pathology.
Keywords	NADPH Oxidase ; NOX ; Superoxide ; Immunity ; Autoimmunity ; COVID-19 ; Medicine (General) ; R5-920 ; Biology (General) ; QH301-705.5
Subject code	572
Language	English
Publishing date	2021-12-01T00:00:00Z
Publisher	Elsevier
Document type	Article ; Online
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Article ; Online: Orthognathic Considerations of Maxillary and Mandibular Asymmetry at Skeletal Maturity in Patients with Cleft Lip and Palate.

Salinero, Lauren K / Friedman, Leigh / Shulkin, Jared M / Barrero, Carlos E / Wagner, Connor S / Pontell, Matthew E / Swanson, Jordan W / Bartlett, Scott P / Nah, Hyun-Duck / Taylor, Jesse A

Plastic and reconstructive surgery

2024

Abstract: ... in ramus length, discrepancy in mandibular body length, and discrepancy in condylar volume (p<0.05 ... Bilateral and unilateral CLP did not show significantly different asymmetry on any measure (p>0.05 ...

Abstract	Background: Improving occlusion and aesthetics is the primary objective of orthognathic surgery for patients with cleft lip and palate (CLP). However, these patients often suffer from horizontal, vertical, and rotational asymmetry in addition to maxillary retrusion. This study aims to describe maxillary and mandibular asymmetry in patients with CLP undergoing orthognathic surgery and analyze its anatomic basis. Methods: Patients with isolated CLP undergoing CT imaging prior to orthognathic surgery were retrospectively reviewed. Maxillary and mandibular positioning and dimensional symmetry were evaluated. Incidence of clinically significant asymmetry, correlations between areas of asymmetry, and associations with clinical history were analyzed. Results: Fifty-eight patients, with mean age 17 years were analyzed, including 32 patients with unilateral CLP and 26 with bilateral CLP. Twenty (34%) patients demonstrated chin deviation ≥4mm and 21 (36%) had a ≥5% discrepancy in mandibular ramus lengths. Horizontal occlusal plane cant of ≥2° was seen in 20 (34%) maxillae and 28 (48%) mandibles, with dental arch yaw ≥2° noted in 32 (55%) of both maxillae and mandibles. Chin deviation correlated with maxillary cant, discrepancy in ramus length, discrepancy in mandibular body length, and discrepancy in condylar volume (p<0.05). Bilateral and unilateral CLP did not show significantly different asymmetry on any measure (p>0.05). Conclusions: Both maxillary and mandibular asymmetry is common in skeletally mature patients with CLP and frequently results in notable chin deviation. Preoperative three-dimensional imaging and virtual surgical planning of orthognathic surgery aid in recognition of facial asymmetries and reveal opportunities to optimize results in this population.
Language	English
Publishing date	2024-04-09
Publishing country	United States
Document type	Journal Article
ZDB-ID	208012-6
ISSN	1529-4242 ; 0032-1052 ; 0096-8501
ISSN (online)	1529-4242
ISSN	0032-1052 ; 0096-8501
DOI	10.1097/PRS.0000000000011463
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Article ; Online: Predictive Dosimetry and Outcomes of Hepatocellular Carcinoma Treated by Yttrium-90 Resin Microsphere Radioembolization: A Retrospective Analysis Using Technetium-99m Macroaggregated Albumin SPECT/CT and Planning Software.

Doyle, Patrick W / Workman, C Spencer / Grice, Jared V / McGonigle, Trey W / Huang, Shi / Borgmann, Anthony J / Baker, Jennifer C / Duncan, David P / Taylor, Jason E / Brown, Daniel B

Journal of vascular and interventional radiology : JVIR

2024 Volume 35, Issue 5, Page(s) 689–698.e3

Abstract: Purpose: To characterize estimated mean absorbed tumor dose (AD: Materials and methods: In this retrospective, single-center study, multicompartment dosimetry of index tumors receiving : Results: The median follow-up period was 148 days ( ... ...

Abstract	Purpose: To characterize estimated mean absorbed tumor dose (AD Materials and methods: In this retrospective, single-center study, multicompartment dosimetry of index tumors receiving Results: The median follow-up period was 148 days (interquartile range [IQR], 92-273 days). The median AD Conclusions: For HCC treated with resin microspheres, tumors receiving higher AD
MeSH term(s)	Humans ; Carcinoma, Hepatocellular/diagnostic imaging ; Carcinoma, Hepatocellular/therapy ; Carcinoma, Hepatocellular/radiotherapy ; Carcinoma, Hepatocellular/pathology ; Liver Neoplasms/diagnostic imaging ; Liver Neoplasms/radiotherapy ; Liver Neoplasms/therapy ; Liver Neoplasms/pathology ; Liver Neoplasms/mortality ; Retrospective Studies ; Yttrium Radioisotopes/administration & dosage ; Yttrium Radioisotopes/adverse effects ; Male ; Female ; Middle Aged ; Radiopharmaceuticals/administration & dosage ; Radiopharmaceuticals/adverse effects ; Aged ; Embolization, Therapeutic/adverse effects ; Technetium Tc 99m Aggregated Albumin/administration & dosage ; Treatment Outcome ; Microspheres ; Single Photon Emission Computed Tomography Computed Tomography ; Predictive Value of Tests ; Time Factors ; Radiotherapy Planning, Computer-Assisted ; Aged, 80 and over ; Software ; Radiotherapy Dosage ; Adult
Chemical Substances	Yttrium Radioisotopes ; Radiopharmaceuticals ; Technetium Tc 99m Aggregated Albumin ; Yttrium-90 (1K8M7UR6O1)
Language	English
Publishing date	2024-01-19
Publishing country	United States
Document type	Journal Article
ZDB-ID	1137756-2
ISSN	1535-7732 ; 1051-0443
ISSN (online)	1535-7732
ISSN	1051-0443
DOI	10.1016/j.jvir.2023.11.026
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Article ; Online: Predictive Partition Dosimetry and Outcomes after Yttrium-90 Resin Microsphere Radioembolization of Colorectal Cancer Metastatic to the Liver: A Retrospective Analysis.

Doyle, Patrick W / Workman, C Spencer / Shah, Neal / McGonigle, Trey W / Grice, Jared V / Huang, Shi / Borgmann, Anthony J / Baker, Jennifer C / Guys, Nicholas P / Taylor, Jason E / Brown, Daniel B

Journal of vascular and interventional radiology : JVIR

2023 Volume 34, Issue 12, Page(s) 2138–2146

Abstract: Purpose: To characterize estimated absorbed tumor dose (AD: Materials and methods: In this retrospective, single-center study, multicompartment dosimetry of index tumors undergoing : Results: Patients had a median follow-up of 116 days ( ... ...

Abstract	Purpose: To characterize estimated absorbed tumor dose (AD Materials and methods: In this retrospective, single-center study, multicompartment dosimetry of index tumors undergoing Results: Patients had a median follow-up of 116 days (interquartile range [IQR], 69-231 days). The AD Conclusions: Tumor dose was the strongest predictor of OR for mCRC. Administration of an estimated 120 Gy to mCRC predicted 55% OR with
MeSH term(s)	Humans ; Female ; Microspheres ; Retrospective Studies ; Technetium Tc 99m Aggregated Albumin ; Liver Neoplasms/diagnostic imaging ; Liver Neoplasms/radiotherapy ; Yttrium Radioisotopes/adverse effects ; Embolization, Therapeutic/adverse effects ; Embolization, Therapeutic/methods ; Colorectal Neoplasms
Chemical Substances	Yttrium-90 (1K8M7UR6O1) ; Technetium Tc 99m Aggregated Albumin ; Yttrium Radioisotopes
Language	English
Publishing date	2023-08-26
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	1137756-2
ISSN	1535-7732 ; 1051-0443
ISSN (online)	1535-7732
ISSN	1051-0443
DOI	10.1016/j.jvir.2023.08.031
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Article ; Online: MDA5-dependent responses contribute to autoimmune diabetes progression and hindrance.

Blum, Samuel I / Taylor, Jared P / Barra, Jessie M / Burg, Ashley R / Shang, Qiao / Qiu, Shihong / Shechter, Oren / Hayes, Aleah R / Green, Todd J / Geurts, Aron M / Chen, Yi-Guang / Tse, Hubert M

JCI insight

2023 Volume 8, Issue 2

Abstract: Type 1 diabetes (T1D) is an autoimmune disease resulting in pancreatic β cell destruction. Coxsackievirus B3 (CVB3) infection and melanoma differentiation-associated protein 5-dependent (MDA5-dependent) antiviral responses are linked with T1D development. ...

Abstract	Type 1 diabetes (T1D) is an autoimmune disease resulting in pancreatic β cell destruction. Coxsackievirus B3 (CVB3) infection and melanoma differentiation-associated protein 5-dependent (MDA5-dependent) antiviral responses are linked with T1D development. Mutations within IFIH1, coding for MDA5, are correlated with T1D susceptibility, but how these mutations contribute to T1D remains unclear. Utilizing nonobese diabetic (NOD) mice lacking Ifih1 expression (KO) or containing an in-frame deletion within the ATPase site of the helicase 1 domain of MDA5 (ΔHel1), we tested the hypothesis that partial or complete loss-of-function mutations in MDA5 would delay T1D by impairing proinflammatory pancreatic macrophage and T cell responses. Spontaneous T1D developed in female NOD and KO mice similarly, but was significantly delayed in ΔHel1 mice, which may be partly due to a concomitant increase in myeloid-derived suppressor cells. Interestingly, KO male mice had increased spontaneous T1D compared with NOD mice. Whereas NOD and KO mice developed CVB3-accelerated T1D, ΔHel1 mice were protected partly due to decreased type I IFNs, pancreatic infiltrating TNF+ macrophages, IFN-γ+CD4+ T cells, and perforin+CD8+ T cells. Furthermore, ΔHel1 MDA5 protein had reduced ATP hydrolysis compared with wild-type MDA5. Our results suggest that dampened MDA5 function delays T1D, yet loss of MDA5 promotes T1D.
MeSH term(s)	Male ; Female ; Mice ; Animals ; Diabetes Mellitus, Type 1 ; Interferon-Induced Helicase, IFIH1 ; Mice, Inbred NOD ; Pancreas/metabolism ; Macrophages/metabolism
Chemical Substances	Interferon-Induced Helicase, IFIH1 (EC 3.6.4.13)
Language	English
Publishing date	2023-01-24
Publishing country	United States
Document type	Journal Article
ISSN	2379-3708
ISSN (online)	2379-3708
DOI	10.1172/jci.insight.157929
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Article: GABA and Combined GABA with GAD65-Alum Treatment Alters Th1 Cytokine Responses of PBMCs from Children with Recent-Onset Type 1 Diabetes.

Heath, Katie E / Feduska, Joseph M / Taylor, Jared P / Houp, Julie A / Botta, Davide / Lund, Frances E / Mick, Gail J / McGwin, Gerald / McCormick, Kenneth L / Tse, Hubert M

Biomedicines

2023 Volume 11, Issue 7

Abstract: Type 1 diabetes (T1D) is an autoimmune disease culminating in the destruction of insulin-producing pancreatic cells. There is a need for the development of novel antigen-specific strategies to delay cell destruction, including combinatorial strategies ... ...

Abstract	Type 1 diabetes (T1D) is an autoimmune disease culminating in the destruction of insulin-producing pancreatic cells. There is a need for the development of novel antigen-specific strategies to delay cell destruction, including combinatorial strategies that do not elicit systemic immunosuppression. Gamma-aminobutyric acid (GABA) is expressed by immune cells, β-cells, and gut bacteria and is immunomodulatory. Glutamic-acid decarboxylase 65 (GAD65), which catalyzes GABA from glutamate, is a T1D autoantigen. To test the efficacy of combinatorial GABA treatment with or without GAD65-immunization to dampen autoimmune responses, we enrolled recent-onset children with T1D in a one-year clinical trial (ClinicalTrials.gov NCT02002130) and examined T cell responses. We isolated peripheral blood mononuclear cells and evaluated cytokine responses following polyclonal activation and GAD65 rechallenge. Both GABA alone and GABA/GAD65-alum treatment inhibited Th1 cytokine responses over the 12-month study with both polyclonal and GAD65 restimulation. We also investigated whether patients with HLA-DR3-DQ2 and HLA-DR4-DQ8, the two highest-risk human leukocyte antigen (HLA) haplotypes in T1D, exhibited differences in response to GABA alone and GABA/GAD65-alum. HLA-DR4-DQ8 patients possessed a Th1-skewed response compared to HLA-DR3-DQ2 patients. We show that GABA and GABA/GAD65-alum present an attractive immunomodulatory treatment for children with T1D and that HLA haplotypes should be considered.
Language	English
Publishing date	2023-07-10
Publishing country	Switzerland
Document type	Journal Article
ZDB-ID	2720867-9
ISSN	2227-9059
ISSN	2227-9059
DOI	10.3390/biomedicines11071948
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Article ; Online: A pilot study evaluating the prefeasibility of a behavioral weight loss program in people with multiple sclerosis

Julia S. Cozart / Amanda S. Bruce / Christie Befort / Catherine Siengsukon / Sharon G. Lynch / Stephanie Punt / Stephen Simon / Robin P. Shook / Joanie Huebner / Taylor Bradish / Jade Robichaud / Jared M. Bruce

Preventive Medicine Reports, Vol 36, Iss , Pp 102437- (2023)

2023

Abstract: ... SD = 7.19). Participants who adhered more closely to the self-monitoring guidelines (r = 0.81, p =.02 ... and who averaged higher weekly active minutes (r = 0.91, p =.002) achieved greater percentage ...

Abstract	Weight loss interventions seldom include individuals with neurologic disease. The aims of the present study were to: 1) develop and assess the prefeasibility of a 6-month telehealth behavioral weight loss program for people with multiple sclerosis (MS) and obesity and 2) examine changes in weight loss (primary outcome), physical activity, and fruit/vegetable consumption at follow-up. Participants with obesity and MS engaged in a 24-week weight loss program. Participants followed established diet, exercise, and self-monitoring guidelines and attended weekly online group meetings. Median percentage weight loss was 10.54 % (SD = 7.19). Participants who adhered more closely to the self-monitoring guidelines (r = 0.81, p =.02), and who averaged higher weekly active minutes (r = 0.91, p =.002) achieved greater percentage weight loss. Six of the eight pilot participants achieved clinically meaningful weight loss (>5%) after 6-months.
Keywords	Weight Loss ; Multiple Sclerosis ; Obesity ; Wellness ; Healthy Lifestyle ; Diet ; Medicine ; R
Subject code	796
Language	English
Publishing date	2023-12-01T00:00:00Z
Publisher	Elsevier
Document type	Article ; Online
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Article: A pilot study evaluating the prefeasibility of a behavioral weight loss program in people with multiple sclerosis.

Cozart, Julia S / Bruce, Amanda S / Befort, Christie / Siengsukon, Catherine / Lynch, Sharon G / Punt, Stephanie / Simon, Stephen / Shook, Robin P / Huebner, Joanie / Bradish, Taylor / Robichaud, Jade / Bruce, Jared M

Preventive medicine reports

2023 Volume 36, Page(s) 102437

Abstract: Weight loss interventions seldom include individuals with neurologic disease. The aims of the present study were to: 1) develop and assess the prefeasibility of a 6-month telehealth behavioral weight loss program for people with multiple sclerosis (MS) ... ...

Abstract	Weight loss interventions seldom include individuals with neurologic disease. The aims of the present study were to: 1) develop and assess the prefeasibility of a 6-month telehealth behavioral weight loss program for people with multiple sclerosis (MS) and obesity and 2) examine changes in weight loss (primary outcome), physical activity, and fruit/vegetable consumption at follow-up. Participants with obesity and MS engaged in a 24-week weight loss program. Participants followed established diet, exercise, and self-monitoring guidelines and attended weekly online group meetings. Median percentage weight loss was 10.54 % (
Language	English
Publishing date	2023-09-22
Publishing country	United States
Document type	Journal Article
ZDB-ID	2785569-7
ISSN	2211-3355
ISSN	2211-3355
DOI	10.1016/j.pmedr.2023.102437
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Article ; Online: Social support predicts sleep quality in people with multiple sclerosis during the COVID-19 pandemic.

Harris, Taylor P / Zaeske, Lauren M / Ludwig, Rebecca / Baker, Sara / Lynch, Sharon / Thuringer, Amanda / Bruce, Jared / Siengsukon, Catherine F

Multiple sclerosis and related disorders

2022 Volume 64, Page(s) 103970

Abstract: Background: Poor sleep quality is one of the most prominent patient-reported problems in people with multiple sclerosis (PwMS). The COVID-19 pandemic resulted in PwMS having less contact with physicians, therapists, support groups, and family, which led ...

Abstract	Background: Poor sleep quality is one of the most prominent patient-reported problems in people with multiple sclerosis (PwMS). The COVID-19 pandemic resulted in PwMS having less contact with physicians, therapists, support groups, and family, which led to decreased access to typical supports. The purpose of this study was to assess how social support impacted sleep quality during the COVID-19 pandemic in PwMS within the United States. Methods: Anonymous surveys were utilized to gather data from February - May 2021 from 209 PwMS during their return appointments (face-to-face and virtual) at the University of Kansas Medical Center (KUMC)'s MS Clinic in the United States. SPSS 27 was used to run four regressions in order to determine if social support predicted sleep quality with and without the inclusion of covariates (age, education, disability, anxiety/depression). Results: The results indicate that overall feelings of being socially supported predict sleep quality. Additionally, various facets of social support predict sleep quality, even when controlling for covariates. Interestingly, while depression and anxiety were significant predictors of sleep quality, those constructs do not attenuate the social support-sleep relationship. Conclusion: These findings will provide key information pertaining to the association between social support and sleep in PwMS during COVID-19 where typical supports were limited. Understanding the challenges facing those living with chronic illnesses, specifically PwMS, will help researchers and clinicians alike create interventions to promote social support in the midst of a global pandemic.
MeSH term(s)	COVID-19 ; Humans ; Multiple Sclerosis/complications ; Multiple Sclerosis/epidemiology ; Pandemics ; Sleep Quality ; Social Support
Language	English
Publishing date	2022-06-14
Publishing country	Netherlands
Document type	Journal Article
ZDB-ID	2645330-7
ISSN	2211-0356 ; 2211-0348
ISSN (online)	2211-0356
ISSN	2211-0348
DOI	10.1016/j.msard.2022.103970
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