Example of Journal of Investigative Medicine High Impact Case Reports format
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Example of Journal of Investigative Medicine High Impact Case Reports format Example of Journal of Investigative Medicine High Impact Case Reports format Example of Journal of Investigative Medicine High Impact Case Reports format Example of Journal of Investigative Medicine High Impact Case Reports format Example of Journal of Investigative Medicine High Impact Case Reports format Example of Journal of Investigative Medicine High Impact Case Reports format Example of Journal of Investigative Medicine High Impact Case Reports format
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Example of Journal of Investigative Medicine High Impact Case Reports format Example of Journal of Investigative Medicine High Impact Case Reports format Example of Journal of Investigative Medicine High Impact Case Reports format Example of Journal of Investigative Medicine High Impact Case Reports format Example of Journal of Investigative Medicine High Impact Case Reports format Example of Journal of Investigative Medicine High Impact Case Reports format Example of Journal of Investigative Medicine High Impact Case Reports format
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open access Open Access

Journal of Investigative Medicine High Impact Case Reports — Template for authors

Publisher: SAGE
Categories Rank Trend in last 3 yrs
Safety Research #54 of 88 down down by None rank
Safety, Risk, Reliability and Quality #114 of 165 down down by None rank
Epidemiology #81 of 99 down down by None rank
journal-quality-icon Journal quality:
Medium
calendar-icon Last 4 years overview: 463 Published Papers | 463 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 29/06/2020
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Related Journals

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Journal Performance & Insights

CiteRatio

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

A measure of average citations received per peer-reviewed paper published in the journal.

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

1.0

9% from 2019

CiteRatio for Journal of Investigative Medicine High Impact Case Reports from 2016 - 2020
Year Value
2020 1.0
2019 1.1
2018 3.0
graph view Graph view
table view Table view

0.247

6% from 2019

SJR for Journal of Investigative Medicine High Impact Case Reports from 2018 - 2020
Year Value
2020 0.247
2019 0.262
2018 0.531
graph view Graph view
table view Table view

0.552

7% from 2019

SNIP for Journal of Investigative Medicine High Impact Case Reports from 2018 - 2020
Year Value
2020 0.552
2019 0.592
2018 0.462
graph view Graph view
table view Table view

insights Insights

  • CiteRatio of this journal has decreased by 9% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

insights Insights

  • SJR of this journal has decreased by 6% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has decreased by 7% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Journal of Investigative Medicine High Impact Case Reports

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SAGE

Journal of Investigative Medicine High Impact Case Reports

Approved by publishing and review experts on SciSpace, this template is built as per for Journal of Investigative Medicine High Impact Case Reports formatting guidelines as mentioned in SAGE author instructions. The current version was created on 29 Jun 2020 and has been used by 816 authors to write and format their manuscripts to this journal.

Pathology

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Last updated on
29 Jun 2020
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ISSN
2324-7096
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Open Access
No
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Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
SageV
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Citation Type
Numbered (Superscripted)
25
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Bibliography Example
Blonder GE, Tinkham M and Klapwijk TM. Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and supercurrent conversion. Phys. Rev. B 1982; 25(7): 4515–4532. URL 10.1103/PhysRevB.25.4515.

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.1177/2324709614526702
Intravascular Large B-Cell Lymphoma: A Difficult Diagnostic Challenge.
Maria S. Khan1, Mark McCubbin2, Sucha Nand2

Abstract:

Case Presentation. A 69-year-old Hispanic male, with a past history of diabetes and coronary disease, was admitted for fever, diarrhea, and confusion of 4 weeks duration. Physical examination showed a disoriented patient with multiple ecchymoses, possible ascites, and bilateral scrotal swelling. Hemoglobin was 6.7, prothrombi... Case Presentation. A 69-year-old Hispanic male, with a past history of diabetes and coronary disease, was admitted for fever, diarrhea, and confusion of 4 weeks duration. Physical examination showed a disoriented patient with multiple ecchymoses, possible ascites, and bilateral scrotal swelling. Hemoglobin was 6.7, prothrombin time (PT) 21.4 seconds with international normalized ratio 2.1, partial thromboplastin time (PTT) 55.6 seconds, fibrin split 10 µg/L, and lactate dehydrogenase (LDH) 1231 IU/L. Except for a positive DNA test for Epstein-Barr virus (EBV) infection, extensive diagnostic workup for infections, malignancy, or a neurological cause was negative. Mixing studies revealed a nonspecific inhibitor of PT and PTT but Factor VIII levels were normal. The patient was empirically treated with antibiotics but developed hypotension and died on day 27 of admission. At autopsy, patient was found to have intravascular diffuse large B-cell lymphoma involving skin, testes, lung, and muscles. The malignant cells were positive for CD20, CD791, Mum-1, and Pax-5 and negative for CD3, CD5, CD10, CD30, and Bcl-6. The malignant cells were 100% positive for Ki-67. Discussion. Intravascular large cell B-cell lymphoma (IVLBCL) is rare form of diffuse large B-cell lymphoma and tends to proliferate within small blood vessels, particularly capillaries and postcapillary venules. The cause of its affinity for vascular bed remains unknown. In many reports, IVLBCL was associated with HIV, HHV8, and EBV infections. The fact that our case showed evidence of EBV infection lends support to the association of this diagnosis to viral illness. The available literature on this subject is scant, and in many cases, the diagnosis was made only at autopsy. The typical presentation of this disorder is with B symptoms, progressive neurologic deficits, and skin findings. Bone marrow, spleen, and liver are involved in a minority of patients. Nearly all patients have elevated LDH, and about 65% are anemic. About 20% have hepatic and renal dysfunction. The treatment consists of systemic chemotherapy with cyclophosphamide, doxorubicin, vincristine, prednisone plus rituximab (CHOP-R) and central nervous system prophylaxis. Retrospective data suggests that, with treatment, 51% to 82% of the patients achieve a complete remission and 27% to 56% are alive at 2-year follow-up. Conclusion. IVLBCL is a difficult diagnosis to make as the disease remains confined to the vascular lumen. It may be associated with certain viral illnesses, and this association needs to be explored further. It is important to consider this diagnosis in the appropriate settings because patients may achieve durable remissions with therapy. read more read less

Topics:

Intravascular large B-cell lymphoma (61%)61% related to the paper, B symptoms (55%)55% related to the paper, Rituximab (52%)52% related to the paper, Large cell (52%)52% related to the paper, Lymphoma (50%)50% related to the paper
View PDF
119 Citations
open accessOpen access Journal Article DOI: 10.1177/2324709620976018
COVID-19-Induced Acute Bilateral Optic Neuritis.

Abstract:

A 44-year-old male patient with no past medical history presented 2 weeks after seropositive coronavirus disease 2019 (COVID-19) infection with vision problems suggestive of optic neuritis. Radiological testing showed findings suspicious for acute bilateral optic neuritis. The patient had also anti-MOG antibodies. Whether thi... A 44-year-old male patient with no past medical history presented 2 weeks after seropositive coronavirus disease 2019 (COVID-19) infection with vision problems suggestive of optic neuritis. Radiological testing showed findings suspicious for acute bilateral optic neuritis. The patient had also anti-MOG antibodies. Whether this was an optic neuritis due to COVID-19, MOG antibody disease, or an activation of MOG antibody disease by COVID-19 is discussed in this case. read more read less

Topics:

Optic neuritis (71%)71% related to the paper
View PDF
91 Citations
open accessOpen access Journal Article DOI: 10.1177/2324709613480346
Cyclophosphamide-Induced Cardiomyopathy: A Case Report, Review, and Recommendations for Management
Sumandeep Dhesi1, Michael P. Chu1, Gregg Blevins1, Ian Paterson1, Loree Larratt1, Gavin Y. Oudit1, Daniel Kim1

Abstract:

Cyclophosphamide is increasingly used to treat various types of cancers and autoimmune conditions. Higher doses of this drug may produce significant cardiac toxicity, including fatal hemorrhagic myocarditis. In this review, we present a case of cyclophosphamide-induced cardiomyopathy requiring mechanical circulatory support. ... Cyclophosphamide is increasingly used to treat various types of cancers and autoimmune conditions. Higher doses of this drug may produce significant cardiac toxicity, including fatal hemorrhagic myocarditis. In this review, we present a case of cyclophosphamide-induced cardiomyopathy requiring mechanical circulatory support. We also describe the pathophysiology, clinical manifestations, and risk factors for this important clinical entity and propose early detection and management strategies. read more read less

Topics:

Cardiomyopathy (56%)56% related to the paper, Myocarditis (51%)51% related to the paper
View PDF
80 Citations
open accessOpen access Journal Article DOI: 10.1177/2324709614556129
Adolescent Premature Ovarian Insufficiency Following Human Papillomavirus Vaccination: A Case Series Seen in General Practice

Abstract:

Three young women who developed premature ovarian insufficiency following quadrivalent human papillomavirus (HPV) vaccination presented to a general practitioner in rural New South Wales, Australia The unrelated girls were aged 16, 16, and 18 years at diagnosis Each had received HPV vaccinations prior to the onset of ovarian ... Three young women who developed premature ovarian insufficiency following quadrivalent human papillomavirus (HPV) vaccination presented to a general practitioner in rural New South Wales, Australia The unrelated girls were aged 16, 16, and 18 years at diagnosis Each had received HPV vaccinations prior to the onset of ovarian decline Vaccinations had been administered in different regions of the state of New South Wales and the 3 girls lived in different towns in that state Each had been prescribed the oral contraceptive pill to treat menstrual cycle abnormalities prior to investigation and diagnosis Vaccine research does not present an ovary histology report of tested rats but does present a testicular histology report Enduring ovarian capacity and duration of function following vaccination is unresearched in preclinical studies, clinical and postlicensure studies Postmarketing surveillance does not accurately represent diagnoses in adverse event notifications and can neither represent unnotified cases nor compare incident statistics with vaccine course administration rates The potential significance of a case series of adolescents with idiopathic premature ovarian insufficiency following HPV vaccination presenting to a general practice warrants further research Preservation of reproductive health is a primary concern in the recipient target group Since this group includes all prepubertal and pubertal young women, demonstration of ongoing, uncompromised safety for the ovary is urgently required This matter needs to be resolved for the purposes of population health and public vaccine confidence read more read less

Topics:

Premature ovarian insufficiency (58%)58% related to the paper, Premature ovarian failure (54%)54% related to the paper, Vaccination (53%)53% related to the paper, Postmarketing surveillance (51%)51% related to the paper
View PDF
53 Citations
open accessOpen access Journal Article DOI: 10.1177/2324709616674316
Pembrolizumab Therapy Triggering an Exacerbation of Preexisting Autoimmune Disease: A Report of 2 Patient Cases.
Sneha Phadke1, Ramez Ghabour1, Brian L. Swick1, Andrea Swenson1, Mohammed M. Milhem1, Yousef Zakharia1

Abstract:

Historically, metastatic melanoma was uniformly and rapidly lethal, and treatment options were limited. In recent years, however, checkpoint inhibitors have emerged as an accepted standard treatment for patients with advanced melanoma. In clinical trials, these agents have been largely well tolerated and have the potential to... Historically, metastatic melanoma was uniformly and rapidly lethal, and treatment options were limited. In recent years, however, checkpoint inhibitors have emerged as an accepted standard treatment for patients with advanced melanoma. In clinical trials, these agents have been largely well tolerated and have the potential to result in durable responses. Importantly though, one must recognize the unique side effect profile of these therapies, which can trigger or exacerbate underlying autoimmune disease. Whether this autoimmune activation is associated with a clinical response to therapy has been debated, and while not definitive, there is evidence in the literature of a possible association. The 2 cases presented describe this autoimmune phenomenon, along with a review of the existing literature on the relationship between response to immunotherapy and autoimmune side effects. read more read less

Topics:

Autoimmune disease (56%)56% related to the paper, Pembrolizumab (55%)55% related to the paper
View PDF
50 Citations
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Frequently asked questions

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13. What is Sherpa RoMEO Archiving Policy for Journal of Investigative Medicine High Impact Case Reports?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Journal of Investigative Medicine High Impact Case Reports. The table below indicates the level of access a journal has as per Sherpa Romeo's archiving policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

14. What are the most common citation types In Journal of Investigative Medicine High Impact Case Reports?

The 5 most common citation types in order of usage for Journal of Investigative Medicine High Impact Case Reports are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

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