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
1988 1
1993 1
2002 4
2003 2
2004 5
2005 4
2006 8
2007 2
2008 3
2009 3
2010 4
2011 5
2012 5
2013 4
2014 4
2015 3
2016 5
2017 3
2018 3
2019 4
2020 4
2021 5
2022 2
2023 2
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

75 results

Results by year

Filters applied: . Clear all
Page 1
Congenital Myasthenic Syndromes Overview.
Abicht A, Müller JS, Lochmüller H. Abicht A, et al. Among authors: muller js. 2003 May 9 [updated 2021 Dec 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2003 May 9 [updated 2021 Dec 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301347 Free Books & Documents. Review.
Modeling hematopoietic disorders in zebrafish.
Konantz M, Schürch C, Hanns P, Müller JS, Sauteur L, Lengerke C. Konantz M, et al. Among authors: muller js. Dis Model Mech. 2019 Sep 6;12(9):dmm040360. doi: 10.1242/dmm.040360. Dis Model Mech. 2019. PMID: 31519693 Free PMC article. Review.
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
Wiessner M, Maroofian R, Ni MY, Pedroni A, Müller JS, Stucka R, Beetz C, Efthymiou S, Santorelli FM, Alfares AA, Zhu C, Uhrova Meszarosova A, Alehabib E, Bakhtiari S, Janecke AR, Otero MG, Chen JYH, Peterson JT, Strom TM, De Jonghe P, Deconinck T, De Ridder W, De Winter J, Pasquariello R, Ricca I, Alfadhel M, van de Warrenburg BP, Portier R, Bergmann C, Ghasemi Firouzabadi S, Jin SC, Bilguvar K, Hamed S, Abdelhameed M, Haridy NA, Maqbool S, Rahman F, Anwar N, Carmichael J, Pagnamenta A, Wood NW, Tran Mau-Them F, Haack T; Genomics England Research Consortium, PREPARE network; Di Rocco M, Ceccherini I, Iacomino M, Zara F, Salpietro V, Scala M, Rusmini M, Xu Y, Wang Y, Suzuki Y, Koh K, Nan H, Ishiura H, Tsuji S, Lambert L, Schmitt E, Lacaze E, Küpper H, Dredge D, Skraban C, Goldstein A, Willis MJH, Grand K, Graham JM, Lewis RA, Millan F, Duman Ö, Dündar N, Uyanik G, Schöls L, Nürnberg P, Nürnberg G, Catala Bordes A, Seeman P, Kuchar M, Darvish H, Rebelo A, Bouçanova F, Medard JJ, Chrast R, Auer-Grumbach M, Alkuraya FS, Shamseldin H, Al Tala S, Rezazadeh Varaghchi J, Najafi M, Deschner S, Gläser D, Hüttel W, Kruer MC, Kamsteeg EJ, Takiyama Y, Züchner S, Baets J, Synofzik M, Sch… See abstract for full author list ➔ Wiessner M, et al. Among authors: muller js. Brain. 2021 Jun 22;144(5):1422-1434. doi: 10.1093/brain/awab041. Brain. 2021. PMID: 33970200 Free PMC article.
A mathematical model for the two-learners problem.
Müller JS, Vidaurre C, Schreuder M, Meinecke FC, von Bünau P, Müller KR. Müller JS, et al. J Neural Eng. 2017 Jun;14(3):036005. doi: 10.1088/1741-2552/aa620b. Epub 2017 Feb 22. J Neural Eng. 2017. PMID: 28224972
[Value of surgery in the palliative therapy for rectal cancer].
Delgadillo X, Müller JS, Solass W, Reymond MA. Delgadillo X, et al. Among authors: muller js. Zentralbl Chir. 2010 Dec;135(6):523-7. doi: 10.1055/s-0030-1262692. Epub 2010 Dec 13. Zentralbl Chir. 2010. PMID: 21154209 Review. German.
Phenotypic convergence of Menkes and Wilson disease.
Bansagi B, Lewis-Smith D, Pal E, Duff J, Griffin H, Pyle A, Müller JS, Rudas G, Aranyi Z, Lochmüller H, Chinnery PF, Horvath R. Bansagi B, et al. Among authors: muller js. Neurol Genet. 2016 Nov 17;2(6):e119. doi: 10.1212/NXG.0000000000000119. eCollection 2016 Dec. Neurol Genet. 2016. PMID: 27878136 Free PMC article.
75 results