Cited by 15Hemophilia Treatment and ResearchConnective tissue disorders researchPlatelet Disorders and Treatments

Epidemiology of bleeding symptoms and hypermobile Ehlers‐Danlos syndrome in paediatrics

Open access
Hickey, S. E., Varga, E. A., Kerlin, B.·2016·Haemophilia

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1111/hae.13063

Cites

2 of 2 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Hickey reported 7/13 (54%) of a case series of younger patients (9-18 years old) with hEDS per Villefranche criteria with menorrhagia post menarche.

    “Hickey reported 7/13 (54%) of a case series of younger patients (9–18 years old) with hEDS per Villefranche criteria with menorrhagia post menarche.”

    From Pediatric joint hypermobility: a diagnostic framework and narrative review (2023) · cites this paper as [69]

    The study reports patients with hEDS diagnosed using Villefranche criteria and says menstrual bleeding symptoms contributed to elevated bleeding scores (study text; page unavailable). But our copy does not report menorrhagia in 7 of 13 post-menarche patients, and its stated eligibility range is 9–21 years, not 9–18. (LLM, conf=0.82)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 8

  1. [1]Beighton P, De Paepe A, Steinmann B, Tsipouras P, Wenstrup RJ. Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK). Am J Med Genet 1998; 77: 31– 7. 9557891
  2. [2]Anstey A, Mayne K, Winter M, Van de Pette J, Pope FM. Platelet and coagulation studies in Ehlers-Danlos syndrome. Br J Dermatol 1991; 125: 155– 63. 1911298
  3. [3]Bowman M, Riddel J, Rand ML, Tosetto A, Silva M, James PD. Evaluation of the diagnostic utility for von Willebrand disease of a pediatric bleeding questionnaire. J Thromb Haemost 2009; 7: 1418– 21. 19496919
  4. [5]Tosetto A, Rodeghiero F, Castaman G A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD). J Thromb Haemost 2006; 4: 766– 73. 16634745
  5. [6]Robertson JD, Yenson PR, Rand ML Expanded phenotype-genotype correlations in a pediatric population with type 1 von Willebrand disease. J Thromb Haemost 2011; 9: 1752– 60. 21711445
  6. [8]Mast KJ, Nunes ME, Ruymann FB, Kerlin BA. Desmopressin responsiveness in children with Ehlers-Danlos syndrome associated bleeding symptoms. Br J Haematol 2009; 144: 230– 3. 19036109
  7. [9]Jackson SC, Odiaman L, Card RT, van der Bom JG, Poon MC. Suspected collagen disorders in the bleeding disorder clinic: a case-control study. Haemophilia 2013; 246– 50. 23030528
  8. [10]O’Brien SH. Bleeding scores: are they really useful? Hematology Am Soc Hematol Educ Program 2012; 2012: 152– 6. 23233574

Cited by

Sorted by citations

Authors
Hickey, S. E., Varga, E. A., & Kerlin, B.
Affiliations
Nationwide Children's Hospital (US)
Corresponding author
Hickey, S. E.
Venue
Haemophilia
Publisher
Wiley
Published
2016-08-26
Volume
22
Issue
5
Pages
e490-3
ISSN
  • 1351-8216 (ISSN-L)
  • 1365-2516
OpenAlex
W2510717535
Cited by
15
References
2
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2023: 4 · 2022: 2 · 2021: 2 · 2020: 1 · 2019: 1 · 2018: 1
FWCI
0.63
Type
journal article
Language
en
Open access
Locations
  • Haemophilia (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Center for Advancing Translational Sciences (UL1TR001070)
Topics
  • Health Sciences › Medicine › Hematology › Hemophilia Treatment and Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Connective tissue disorders research
  • Health Sciences › Medicine › Hematology › Platelet Disorders and Treatments
Keywords
hypermobile Ehlers-Danlos syndrome, bleeding manifestations, pediatric patients, epidemiology, bleeding complications, connective tissue diseases
MeSH terms
Adolescent, Child, Ehlers-Danlos Syndrome, Female, Hemorrhage, Humans, Male, Surveys and Questionnaires, Cohort Studies

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review