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  1. Article ; Online: Solitary Fibrous Tumor of the Kidney With Pure Round Cell Features: A Case Report With Review of Literature.

    Lobo, Anandi / Jha, Shilpy / Kapoor, Rahul / Diwaker, Preeti / Akgul, Mahmut / Arora, Samriti / Pradhan, Manas / Sahoo, Biswajit / Nigam, Lovelesh K / Mohanty, Sambit K

    International journal of surgical pathology

    2023  Volume 32, Issue 4, Page(s) 851–855

    Abstract: Solitary fibrous tumor (SFT) is a rare mesenchymal neoplasm known to occur at various soft tissue and visceral locations. Kidney is a rarely reported site for these tumors. Most of the SFTs described in the kidney exhibit a classical CD34-positive ... ...

    Abstract Solitary fibrous tumor (SFT) is a rare mesenchymal neoplasm known to occur at various soft tissue and visceral locations. Kidney is a rarely reported site for these tumors. Most of the SFTs described in the kidney exhibit a classical CD34-positive patternless spindle cell histology. Focal round cell morphology is seldom reported. Herein, we describe a 48-year-old male patient with renal SFT. This tumor had pure round cell morphology with a CD34-/STAT6+ immunophenotype. Fluorescent in situ hybridization and a multiplexed sequencing assay performed on an Illumina® HiSeq 4000 platform revealed
    MeSH term(s) Humans ; Solitary Fibrous Tumors/pathology ; Solitary Fibrous Tumors/diagnosis ; Male ; Kidney Neoplasms/pathology ; Kidney Neoplasms/diagnosis ; Middle Aged ; STAT6 Transcription Factor/genetics ; STAT6 Transcription Factor/analysis ; STAT6 Transcription Factor/metabolism ; Biomarkers, Tumor/analysis ; Biomarkers, Tumor/genetics ; Diagnosis, Differential ; Kidney/pathology ; Gene Rearrangement ; Repressor Proteins/genetics ; Repressor Proteins/metabolism ; In Situ Hybridization, Fluorescence ; Antigens, CD34/metabolism ; Antigens, CD34/analysis ; Nephrectomy
    Chemical Substances STAT6 protein, human ; STAT6 Transcription Factor ; Biomarkers, Tumor ; NAB2 protein, human ; Repressor Proteins ; Antigens, CD34
    Language English
    Publishing date 2023-09-16
    Publishing country United States
    Document type Case Reports ; Journal Article ; Review
    ZDB-ID 1336393-1
    ISSN 1940-2465 ; 1066-8969
    ISSN (online) 1940-2465
    ISSN 1066-8969
    DOI 10.1177/10668969231199165
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: SS18-SSX Expression in a Contemporary Cohort of Primary Renal Synovial Sarcoma: A Multi-Institutional Experience of Fourteen Patients.

    Challa, Bindu / Mohanty, Sambit K / Jha, Shilpy / Sampat, Nakul Y / Sardana, Ruhani / Lobo, Anandi / Sharma, Shivani / Arora, Samriti / Rath, Debadarshi / Munjal, Gauri / Pattnaik, Niharika / Jain, Deepika / Jain, Ekta / Dewan, Aditi / Dixit, Mallika / Malik, Vipra / Shinde, Sayali / Balzer, Bonnie L / Parwani, Anil

    International journal of surgical pathology

    2023  Volume 31, Issue 7, Page(s) 1232–1243

    Abstract: Primary renal synovial sarcoma is a rare aggressive mesenchymal neoplasm of the kidney that accounts for less than 1% of renal sarcomas. Herein, we describe the clinicopathologic and molecular findings of 14 renal synovial sarcoma patients in one of the ... ...

    Abstract Primary renal synovial sarcoma is a rare aggressive mesenchymal neoplasm of the kidney that accounts for less than 1% of renal sarcomas. Herein, we describe the clinicopathologic and molecular findings of 14 renal synovial sarcoma patients in one of the largest case series to date and to our knowledge, the only renal synovial sarcoma series to use novel SS18-SSX IHC. Clinicopathologic, IHC, molecular, management, and follow-up data were reviewed and analyzed. Macroscopically, the tumors had either homogeneous, tan-white, and solid (
    MeSH term(s) Humans ; Sarcoma, Synovial/diagnosis ; Sarcoma, Synovial/genetics ; Oncogene Proteins, Fusion/genetics ; Lung/pathology
    Chemical Substances Oncogene Proteins, Fusion
    Language English
    Publishing date 2023-01-02
    Publishing country United States
    Document type Multicenter Study ; Journal Article
    ZDB-ID 1336393-1
    ISSN 1940-2465 ; 1066-8969
    ISSN (online) 1940-2465
    ISSN 1066-8969
    DOI 10.1177/10668969221143481
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Evaluation of programmed cell death ligand 1 expression in a contemporary cohort of penile squamous cell carcinoma and its correlation with clinicopathologic and survival parameters: A study of 134 patients.

    Lobo, Anandi / Mishra, Sourav K / Jha, Shilpy / Tiwari, Ankit / Kapoor, Rahul / Sharma, Shivani / Kaushal, Seema / Kiranmai, N Sri / Das, M Rakshitha / Peddinti, Kamal P / Sharma, Shailendra K / Bhardwaj, Nitin / Arora, Samriti / Jain, Deepika / Jain, Ekta / Munjal, Gauri / Shinde, Sayali / Malik, Vipra / Singh, Hena /
    Varshney, Juhi / Pradhan, Dinesh / Dixit, Mallika / Pattnaik, Niharika / Sharma, Ashish K / Barapatre, Yogesh R / Pradhan, Manas / Satapathy, Kaliprasad / Rath, Debadarshi / Jaiswal, Sunil / Das, Stithi / Khadenga, Chiraranjan / Routa, Sudhasmita / Baisakh, Manas R / Tiwari, Romila / Sampat, Nakul Y / Chakrabarti, Indranil / Parwani, Anil V / Mohanty, Sambit K

    American journal of clinical pathology

    2024  Volume 161, Issue 1, Page(s) 49–59

    Abstract: Objectives: Penile squamous cell carcinomas (PCs) are rare malignancies with a dismal prognosis in a metastatic setting; therefore, novel immunotherapeutic modalities are an unmet need. One such modality is the immune checkpoint molecule programmed cell ...

    Abstract Objectives: Penile squamous cell carcinomas (PCs) are rare malignancies with a dismal prognosis in a metastatic setting; therefore, novel immunotherapeutic modalities are an unmet need. One such modality is the immune checkpoint molecule programmed cell death ligand 1 (PD-L1). We sought to analyze PD-L1 expression and its correlation with various clinicopathologic parameters in a contemporary cohort of 134 patients with PC.
    Methods: A cohort of 134 patients with PC was studied for PD-L1 immunohistochemistry. The PD-L1 expression was evaluated using a combined proportion score with a cutoff of 1 or higher to define positivity. The results were correlated with various clinicopathologic parameters.
    Results: Overall, 77 (57%) patients had positive PD-L1 expression. Significantly high PD-L1 expression was observed in high-grade tumors (P = .006). We found that 37% of human papillomavirus (HPV)-associated subtypes and 73% of other histotype tumors expressed PD-L1, while 63% of HPV-associated tumors and 27% of other histotype tumors did not (odds ratio, 1.35; P = .002 when compared for HPV-associated groups vs all others). Similarly, PD-L1-positive tumors had a 3.61-times higher chance of being node positive than PD-L1-negative tumors (P = .0009). In addition, PD-L1 high-positive tumors had a 5-times higher chance of being p16ink4a negative than PD-L1 low-positive tumors (P = .004). The PD-L1-positive tumors had a lower overall survival and cancer-specific survival than PD-L1-negative tumors.
    Conclusions: Overall, PD-L1 expression is associated with high-grade and metastatic tumors. Lower PD-L1 expression is observed more frequently in HPV-associated (warty or basaloid) subtypes than in other, predominantly HPV-independent types. As a result, PD-L1 positivity, including higher expression, portends lower overall and cancer-specific survival. These data provide a rational for further investigating PD-L1-based immunotherapeutics in PC.
    MeSH term(s) Male ; Humans ; Papillomavirus Infections/complications ; Papillomavirus Infections/metabolism ; B7-H1 Antigen/metabolism ; Ligands ; Prognosis ; Carcinoma, Squamous Cell/pathology ; Penile Neoplasms/pathology ; Apoptosis ; Biomarkers, Tumor/metabolism
    Chemical Substances B7-H1 Antigen ; Ligands ; Biomarkers, Tumor
    Language English
    Publishing date 2024-01-01
    Publishing country England
    Document type Journal Article
    ZDB-ID 2944-0
    ISSN 1943-7722 ; 0002-9173
    ISSN (online) 1943-7722
    ISSN 0002-9173
    DOI 10.1093/ajcp/aqad107
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Diagnostic Utility of GATA3 and ISL1 in Differentiating Neuroblastoma From Other Pediatric Malignant Small Round Blue Cell Tumors.

    Mohanty, Sambit K / Diwaker, Preeti / Mishra, Sourav K / Jha, Shilpy / Lobo, Anandi / Panda, Saroj P / Sharma, Shivani / Kumar, Mohit / Arora, Samriti / Mallik, Vipra / Jain, Deepika / Jain, Ekta / Chakrabarti, Indranil / Varshney, Juhi / Beg, Arshi / Dixit, Mallika / Baisakh, Manas R / Naik, Subhasini / Sahoo, Subrat K /
    Akgul, Mahmut / Balzer, Bonnie L / Amin, Mahul B / Parwani, Anil V

    International journal of surgical pathology

    2023  Volume 32, Issue 2, Page(s) 294–303

    Abstract: Accurate diagnosis of neuroblastoma may be challenging, especially with limited or inadequate specimen and at the metastatic sites due to overlapping imaging, histopathologic, and immunohistochemical (immunohistochemistry [IHC]; infidelity among various ... ...

    Abstract Accurate diagnosis of neuroblastoma may be challenging, especially with limited or inadequate specimen and at the metastatic sites due to overlapping imaging, histopathologic, and immunohistochemical (immunohistochemistry [IHC]; infidelity among various lineage-associated transcription factors eg FLI1, transducin-like enhancer 1, etc) features. GATA3 and ISL1 have recently been described as markers of neuroblastic differentiation. This study aims at determining the diagnostic utility of GATA3 and ISL1 in differentiating neuroblastoma from other pediatric malignant small round blue cell tumors.
    We evaluated GATA3 and ISL1 expression in 74 pediatric small round blue cell tumors that included 23
    All 23 neuroblastomas (moderate to strong staining in >50% of the tumor cells), 5 T-lymphoblastic lymphomas (moderate to strong staining in 40%-90% of the tumor cells), and 2 desmoplastic small round cell tumors (weak to moderate staining in 20%-30% of the tumor cells) expressed GATA3, while other tumors were negative. ISL1 immunoreactivity was observed in 22 (96%) neuroblastomas (strong staining in in >50% of the tumor cells, n  =  17; moderate to strong staining in 26%-50% of the tumor cells, n  =  5), 3 embryonal rhabdomyosarcoma (moderate to strong staining in 30%-85% of the tumor cells), 1 synovial sarcoma (weak staining in 20% of the tumor cells), and 7 medulloblastoma (strong staining in 60%-90% of the tumor cells). Other tumors were negative. Overall, GATA3 showed 86% specificity, 100% sensitivity, and 90% accuracy for neuroblastoma, with a positive predictive value (PPV) and negative predictive value (NPV) of 77% and 100%, respectively. ISLI showed 72% specificity, 96% sensitivity, and 81% accuracy for neuroblastoma, with a PPV and NPV of 67% and 97%, respectively. After the exclusion of T-lymphoblastic lymphoma and desmoplastic small round cell tumors, GATA3 had 100% specificity, sensitivity, accuracy, and PPV and NPV for neuroblastoma. Similarly, in pediatric small round blue cell tumors, ISL1 had 100% specificity, sensitivity, accuracy, PPV, and NPV for neuroblastoma, after embryonal rhabdomyosarcoma, synovial sarcoma, and medulloblastoma were excluded.
    Conclusions: GATA3 and ISL1 may be valuable in the diagnostic work-up of neuroblastoma and may reliably be used to support the neuroblastic lineage of pediatric small round blue cell tumors. Furthermore, dual positivity helps in challenging scenarios, when there is equivocal imaging, overlapping IHC features, limited specimen, and the lack of facility for a molecular work up.
    MeSH term(s) Humans ; Child ; Medulloblastoma ; Sarcoma, Synovial/diagnosis ; Sarcoma, Synovial/genetics ; Rhabdomyosarcoma, Embryonal ; Neuroblastoma/diagnosis ; Wilms Tumor/diagnosis ; Precursor Cell Lymphoblastic Leukemia-Lymphoma ; Cerebellar Neoplasms ; Kidney Neoplasms/diagnosis ; Kidney Neoplasms/genetics ; Biomarkers, Tumor ; Diagnosis, Differential ; GATA3 Transcription Factor
    Chemical Substances Biomarkers, Tumor ; GATA3 protein, human ; GATA3 Transcription Factor
    Language English
    Publishing date 2023-06-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1336393-1
    ISSN 1940-2465 ; 1066-8969
    ISSN (online) 1940-2465
    ISSN 1066-8969
    DOI 10.1177/10668969231177700
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Solitary Fibrous Tumor of the Adrenal Gland.

    Jha, Shilpy / Mohanty, Sambit K / Sampat, Nakul Y / Naik, Subhasini / Baisakh, Manas R / Pattnaik, Niharika / Lobo, Anandi / Rauta, Sudhasmita / Sharma, Shivani / Munjal, Gauri / Jain, Deepika / Arora, Samriti / Malik, Vipra / Jain, Ekta / Sahoo, Biswajit / Bhardwaj, Mohit / Mishra, Saurav K / Jaiswal, Sunil / Barik, Lalit M /
    Balzer, Bonnie L / Chakrabarti, Indranil / Parwani, Anil V

    American journal of clinical pathology

    2022  Volume 158, Issue 4, Page(s) 546–554

    Abstract: Objectives: Solitary fibrous tumor (SFT) is a mesenchymal neoplasm that can arise at various anatomic locations. It is characterized by inv12(q13q13)-derived NAB2::STAT6 fusion, resulting in the nuclear expression of STAT6. Primary SFT of the adrenal ... ...

    Abstract Objectives: Solitary fibrous tumor (SFT) is a mesenchymal neoplasm that can arise at various anatomic locations. It is characterized by inv12(q13q13)-derived NAB2::STAT6 fusion, resulting in the nuclear expression of STAT6. Primary SFT of the adrenal gland is rare. We launched a multi-institutional collaboration to comprehend the overarching demographics, clinical and follow-up, macroscopic, microscopic, IHC, and FISH features of 9 patients with SFT of the adrenal gland.
    Methods: We added a series of 9 patients to the collection of adrenal SFTs where the clinicopathologic parameters, including clinical presentation, imaging, histopathology, IHC, molecular profiles, and management and follow-up data, were analyzed comprehensively. A modified 4-variable risk stratification model, including age, tumor size, and necrosis, was applied.
    Results: Our series consisted of 6 male and 3 female patients, ranging in age from 19 to 64 years (mean, 49.3 years). Abdominal pain (4) and fever with abdominal pain (1) were the presenting symptoms in 5 patients. In the remaining 4 patients, the tumors were detected by abdominal imaging for hypertension and diabetes. The size of the tumor ranged from 2 cm to 10.5 cm in maximum dimension. All tumors exhibited the morphology of a spindle cell SFT with a patternless architecture; 3 had a focal storiform arrangement. STAT6 positivity was observed in all tumors, and 7 were positive for CD34. Surgical resection was the primary modality of treatment. No adjuvant therapy was administered. Follow-up ranging from 7 months to 23 months was available for 7 patients. All were alive without disease recurrence or metastasis. Risk stratification placed 8 (88.9%) patients into a low-risk category and 1 into an intermediate-risk category.
    Conclusions: This series is the largest of adrenal SFTs to date. These tumors of the adrenal gland are predominantly spindle cell neoplasms with indolent behavior, with a wide age distribution and a slight male preponderance. Combining our cohort with the previously published cases, the majority of tumors fall into the low-risk category for the propensity to develop metastases. Owing to the rarity and age distribution associated with these tumors, the differential diagnosis is wide and requires a systematic approach for ruling out key differential diagnoses aided by STAT6 IHC.
    MeSH term(s) Abdominal Pain ; Adrenal Gland Neoplasms/diagnosis ; Adrenal Glands/pathology ; Adult ; Biomarkers, Tumor/metabolism ; Female ; Humans ; Immunohistochemistry ; Male ; Middle Aged ; Neoplasm Recurrence, Local/pathology ; Repressor Proteins/metabolism ; STAT6 Transcription Factor/genetics ; Severe Fever with Thrombocytopenia Syndrome ; Solitary Fibrous Tumors/diagnosis ; Solitary Fibrous Tumors/pathology ; Young Adult
    Chemical Substances Biomarkers, Tumor ; Repressor Proteins ; STAT6 Transcription Factor
    Language English
    Publishing date 2022-12-02
    Publishing country England
    Document type Journal Article ; Multicenter Study
    ZDB-ID 2944-0
    ISSN 1943-7722 ; 0002-9173
    ISSN (online) 1943-7722
    ISSN 0002-9173
    DOI 10.1093/ajcp/aqac088
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Ud II Zs.91: Show issues Location:
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  6. Article ; Online: Multifaceted Spindle Cell/Sclerosing Rhabdomyosarcoma With Role of Immunohistochemistry in Avoiding Misdiagnosis: A Multi-Institutional Study of 45 Distinct Tumors.

    Jain, Ekta / Munjal, Gauri / Sharma, Shivani / Brar, Zoya / Bhardwaj, Nitin / Dewan, Aditi / Jain, Deepika / Jha, Shilpy / Lobo, Anandi / Malik, Vipra / Arora, Samriti / Varshney, Juhi / Beg, Arshi / Sampat, Nakul Y / Parwani, Anil V / Balzer, Bonnie / Varma, Monica / Yadav, Brijpal S / Sharma, Shailendra K /
    Singh, Hena Paul / Gogoi, Kamakhya / Kumar, Devendra / Bhandari, Vijinder / Fulara, Lalit M / Kumar, Arvind / Singh, Harish / Bhattacharya, Munmun / Dixit, Mallika / Mohanty, Sambit K

    International journal of surgical pathology

    2023  Volume 32, Issue 3, Page(s) 496–506

    Abstract: Background. ...

    Abstract Background.
    MeSH term(s) Adult ; Child ; Adolescent ; Humans ; Male ; Female ; Infant ; Child, Preschool ; Young Adult ; Middle Aged ; Aged ; Aged, 80 and over ; Immunohistochemistry ; Sclerosis/pathology ; Rhabdomyosarcoma/diagnosis ; Rhabdomyosarcoma/pathology ; Muscle, Skeletal/pathology ; Neurofibrosarcoma ; Biomarkers, Tumor
    Chemical Substances Biomarkers, Tumor
    Language English
    Publishing date 2023-07-25
    Publishing country United States
    Document type Multicenter Study ; Journal Article
    ZDB-ID 1336393-1
    ISSN 1940-2465 ; 1066-8969
    ISSN (online) 1940-2465
    ISSN 1066-8969
    DOI 10.1177/10668969231188422
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Reporting Trends, Practices, and Resource Utilization in Neuroendocrine Tumors of the Prostate Gland: A Survey among Thirty-Nine Genitourinary Pathologists.

    Mohanty, Sambit K / Lobo, Anandi / Williamson, Sean R / Shah, Rajal B / Trpkov, Kiril / Varma, Murali / Sirohi, Deepika / Aron, Manju / Kandukari, Shivani R / Balzer, Bonnie L / Luthringer, Daniel L / Ro, Jae / Osunkoya, Adeboye O / Desai, Sangeeta / Menon, Santosh / Nigam, Lovelesh K / Sardana, Rohan / Roy, Paromita / Kaushal, Seema /
    Midha, Divya / Swain, Minakshi / Ambekar, Asawari / Mitra, Suvradeep / Rao, Vishal / Soni, Shailesh / Jain, Kavita / Diwaker, Preeti / Pattnaik, Niharika / Sharma, Shivani / Chakrabarti, Indranil / Sable, Mukund / Jain, Ekta / Jain, Deepika / Samra, Spinder / Vankalakunti, Mahesha / Mohanty, Subhashis / Parwani, Anil V / Sancheti, Sankalp / Kumari, Niraj / Jha, Shilpy / Dixit, Mallika / Malik, Vipra / Arora, Samriti / Munjal, Gauri / Gopalan, Anuradha / Magi-Galluzzi, Cristina / Dhillon, Jasreman

    International journal of surgical pathology

    2022  Volume 31, Issue 6, Page(s) 993–1005

    Abstract: Background. ...

    Abstract Background.
    MeSH term(s) Male ; Humans ; Prostate/pathology ; Neuroendocrine Tumors/diagnosis ; Neuroendocrine Tumors/pathology ; Pathologists ; Prostatic Neoplasms/diagnosis ; Prostatic Neoplasms/pathology ; Carcinoma, Neuroendocrine/pathology ; Carcinoma, Small Cell/pathology ; Carcinoma, Acinar Cell/pathology ; Carcinoma, Large Cell/pathology ; Surveys and Questionnaires
    Language English
    Publishing date 2022-08-09
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1336393-1
    ISSN 1940-2465 ; 1066-8969
    ISSN (online) 1940-2465
    ISSN 1066-8969
    DOI 10.1177/10668969221116629
    Database MEDical Literature Analysis and Retrieval System OnLINE

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