Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 5
1991 1
1995 1
1999 1
2001 1
2002 1
2004 2
2005 1
2006 2
2007 1
2008 1
2009 2
2010 3
2011 2
2012 1
2014 1
2015 2
2017 1
2018 1
2020 6
2021 1
2022 1
2023 1
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

36 results

Results by year

Filters applied: . Clear all
Page 1
New findings in oligogenic inheritance of congenital hypogonadotropic hypogonadism.
Gach A, Pinkier I, Wysocka U, Sałacińska K, Salachna D, Szarras-Czapnik M, Pietrzyk A, Sakowicz A, Nykel A, Rutkowska L, Rybak-Krzyszkowska M, Socha M, Jamsheer A, Jakubowski L. Gach A, et al. Among authors: szarras czapnik m. Arch Med Sci. 2020 Sep 18;18(2):353-364. doi: 10.5114/aoms.2020.98909. eCollection 2022. Arch Med Sci. 2020. PMID: 35316923 Free PMC article.
Endocrine disorders in a patient with a suspicion of a mitochondrial disease, MELAS syndrome - a case report and literature review.
Baszyńska-Wilk M, Moszczyńska E, Szarras-Czapnik M, Wysocka-Mincewicz M, Wątrobińska U, Kozłowska A, Szalecki M. Baszyńska-Wilk M, et al. Among authors: szarras czapnik m. Pediatr Endocrinol Diabetes Metab. 2021;27(3):213-218. doi: 10.5114/pedm.2021.107713. Pediatr Endocrinol Diabetes Metab. 2021. PMID: 34596368 Free PMC article. Review.
Risk of gonadal neoplasia in patients with disorders/differences of sex development.
Slowikowska-Hilczer J, Szarras-Czapnik M, Duranteau L, Rapp M, Walczak-Jedrzejowska R, Marchlewska K, Oszukowska E, Nordenstrom A; dsd-LIFE group. Slowikowska-Hilczer J, et al. Among authors: szarras czapnik m. Cancer Epidemiol. 2020 Dec;69:101800. doi: 10.1016/j.canep.2020.101800. Epub 2020 Sep 6. Cancer Epidemiol. 2020. PMID: 32905884
Volume of the normal prostate gland in polish boys, aged 1-17 years: Based on transabdominal ultrasound - Prospective study.
Kowalczyk K, Gołuch M, Armata M, Rycielski P, Jurkiewicz E, Szarras-Czapnik M, Gogolewski M, Skobejko-Włodarska L, Strulak K, Oskroba K, Felberg K, Gastoł P. Kowalczyk K, et al. Among authors: szarras czapnik m. J Pediatr Urol. 2023 Dec 16:S1477-5131(23)00563-6. doi: 10.1016/j.jpurol.2023.12.007. Online ahead of print. J Pediatr Urol. 2023. PMID: 38158283
Identification of gene variants in a cohort of hypogonadotropic hypogonadism: Diagnostic utility of custom NGS panel and WES in unravelling genetic complexity of the disease.
Gach A, Pinkier I, Sałacińska K, Szarras-Czapnik M, Salachna D, Kucińska A, Rybak-Krzyszkowska M, Sakowicz A. Gach A, et al. Among authors: szarras czapnik m. Mol Cell Endocrinol. 2020 Nov 1;517:110968. doi: 10.1016/j.mce.2020.110968. Epub 2020 Aug 4. Mol Cell Endocrinol. 2020. PMID: 32763379
Response to the attached letter to the Editor regarding the article to "Volume of the normal prostate gland in polish boys, aged 1-17 years: Based on transabdominal ultrasound - Prospective study".
Kowalczyk K, Gołuch M, Armata M, Rycielski P, Jurkiewicz E, Szarras-Czapnik M, Gogolewski M, Skobejko-Włodarska L, Strulak K, Oskroba K, Felberg K, Gastoł P. Kowalczyk K, et al. Among authors: szarras czapnik m. J Pediatr Urol. 2024 Feb 10:S1477-5131(24)00079-2. doi: 10.1016/j.jpurol.2024.02.003. Online ahead of print. J Pediatr Urol. 2024. PMID: 38403512 No abstract available.
Familial X/Y translocations associated with variable sexual phenotype.
Sharp A, Kusz K, Jaruzelska J, Szarras-Czapnik M, Wolski J, Jacobs P. Sharp A, et al. Among authors: szarras czapnik m. J Med Genet. 2004 Jun;41(6):440-4. doi: 10.1136/jmg.2003.017624. J Med Genet. 2004. PMID: 15173229 Free PMC article. No abstract available.
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.
Krone N, Reisch N, Idkowiak J, Dhir V, Ivison HE, Hughes BA, Rose IT, O'Neil DM, Vijzelaar R, Smith MJ, MacDonald F, Cole TR, Adolphs N, Barton JS, Blair EM, Braddock SR, Collins F, Cragun DL, Dattani MT, Day R, Dougan S, Feist M, Gottschalk ME, Gregory JW, Haim M, Harrison R, Olney AH, Hauffa BP, Hindmarsh PC, Hopkin RJ, Jira PE, Kempers M, Kerstens MN, Khalifa MM, Köhler B, Maiter D, Nielsen S, O'Riordan SM, Roth CL, Shane KP, Silink M, Stikkelbroeck NM, Sweeney E, Szarras-Czapnik M, Waterson JR, Williamson L, Hartmann MF, Taylor NF, Wudy SA, Malunowicz EM, Shackleton CH, Arlt W. Krone N, et al. Among authors: szarras czapnik m. J Clin Endocrinol Metab. 2012 Feb;97(2):E257-67. doi: 10.1210/jc.2011-0640. Epub 2011 Dec 7. J Clin Endocrinol Metab. 2012. PMID: 22162478 Free PMC article.
36 results