Article in Current issues in molecular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
2 · The registry
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what money
Authors and funding
9 authors.
Irene FylaktouDivision of Endocrinology, Diabetes and Metabolism 'Aghia Sophia' Children's Hospital ENDO-ERN Center for Rare Paediatric Endocrine Diseases, First Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, 'Aghia Sophia' Children's Hospital, 11527 Athens, Greece.ORCID 0000-0002-4501-4815
Anny MertzanianDivision of Endocrinology, Diabetes and Metabolism 'Aghia Sophia' Children's Hospital ENDO-ERN Center for Rare Paediatric Endocrine Diseases, First Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, 'Aghia Sophia' Children's Hospital, 11527 Athens, Greece.
Ioanna FaraklaDivision of Endocrinology, Diabetes and Metabolism 'Aghia Sophia' Children's Hospital ENDO-ERN Center for Rare Paediatric Endocrine Diseases, First Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, 'Aghia Sophia' Children's Hospital, 11527 Athens, Greece.
Alexandros GryparisDepartment of Speech and Language Therapy, School of Health Sciences, University of Ioannina, 45110 Ioannina, Greece.ORCID 0000-0003-0563-0282
Ioannis Anargyros VasilakisDivision of Endocrinology, Diabetes and Metabolism 'Aghia Sophia' Children's Hospital ENDO-ERN Center for Rare Paediatric Endocrine Diseases, First Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, 'Aghia Sophia' Children's Hospital, 11527 Athens, Greece.
Maria BinouDivision of Endocrinology, Diabetes and Metabolism 'Aghia Sophia' Children's Hospital ENDO-ERN Center for Rare Paediatric Endocrine Diseases, First Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, 'Aghia Sophia' Children's Hospital, 11527 Athens, Greece.ORCID 0000-0002-0115-6934
Evangelia CharmandariDivision of Endocrinology, Diabetes and Metabolism 'Aghia Sophia' Children's Hospital ENDO-ERN Center for Rare Paediatric Endocrine Diseases, First Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, 'Aghia Sophia' Children's Hospital, 11527 Athens, Greece.ORCID 0000-0002-0851-6998
Christina Kanaka-GantenbeinDivision of Endocrinology, Diabetes and Metabolism 'Aghia Sophia' Children's Hospital ENDO-ERN Center for Rare Paediatric Endocrine Diseases, First Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, 'Aghia Sophia' Children's Hospital, 11527 Athens, Greece.ORCID 0000-0001-6942-6470
Amalia SertedakiDivision of Endocrinology, Diabetes and Metabolism 'Aghia Sophia' Children's Hospital ENDO-ERN Center for Rare Paediatric Endocrine Diseases, First Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, 'Aghia Sophia' Children's Hospital, 11527 Athens, Greece.ORCID 0000-0002-3648-3812
Funding
No grant is acknowledged in the PubMed record.
6 · The paper itself
Abstract
21-hydroxylase deficiency (21-OHD) represents the most common form of congenital adrenal hyperplasia (CAH) due to
Indexed as
17-hydroxyprogesterone21-hydroxylase deficiencycongenital adrenal hyperplasiaCYP21A2 genede novo aberrationspathogenic variants
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.
Genetics of 21-OH Deficiency and Genotype-Phenotype Correlation: Experience of the Hellenic National Referral Center. · full record | OpenQuestion