Noonans syndrom (Swedish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Noonans syndrom" in Swedish language version.

refsWebsite

Global rank Swedish rank

10doi.org

2^nd place

14^th place

6worldcat.org

5^th place

9^th place

3nih.gov

4^th place

17^th place

2elsevier.com

610^th place

590^th place

1socialstyrelsen.se

low place

189^th place

1medlineplus.gov

1,581^st place

457^th place

1karger.com

4,489^th place

2,913^th place

1agrenska.se

low place

1rarediseases.org

5,181^st place

4,502^nd place

1nature.com

234^th place

206^th place

1biomedcentral.com

2,747^th place

1,030^th place

1bmj.com

1,226^th place

1,106^th place

1noonan.nu

low place

agrenska.se

Ågrenska (2021). ”Noonans syndrom - Familjevistelse 2021 [PDF].”. https://www.agrenska.se/globalassets/agrenska.se/pdf/dokumentationer/01.familjevistelse-tga/noonans-syndrom-2021-familjevistelse.pdf.

biomedcentral.com

bmcpediatr.biomedcentral.com

Baldo, Francesco; Fachin, Alice; Da Re, Beatrice; Rubinato, Elisa; Bobbo, Marco; Barbi, Egidio (2022-12-24). ”New insights on Noonan syndrome’s clinical phenotype: a single center retrospective study” (på engelska). BMC Pediatrics 22 (1). doi:10.1186/s12887-022-03804-2. ISSN 1471-2431. https://bmcpediatr.biomedcentral.com/articles/10.1186/s12887-022-03804-2. Läst 20 maj 2024.

bmj.com

adc.bmj.com

Zenker, Martin; Edouard, Thomas; Blair, Joanne C; Cappa, Marco (2022-12). ”Noonan syndrome: improving recognition and diagnosis” (på engelska). Archives of Disease in Childhood 107 (12): sid. 1073–1078. doi:10.1136/archdischild-2021-322858. ISSN 0003-9888. https://adc.bmj.com/lookup/doi/10.1136/archdischild-2021-322858. Läst 20 maj 2024.

doi.org

dx.doi.org

Jorge, Alexander A.L.; Malaquias, Alexsandra C.; Arnhold, Ivo J.P.; Mendonca, Berenice B. (2009). ”Noonan Syndrome and Related Disorders: A Review of Clinical Features and Mutations in Genes of the RAS/MAPK Pathway” (på engelska). Hormone Research in Paediatrics 71 (4): sid. 185–193. doi:10.1159/000201106. ISSN 1663-2818. https://karger.com/HRE/article/doi/10.1159/000201106. Läst 19 maj 2024.
Croonen, Ellen A; Nillesen, Willy M; Stuurman, Kyra E; Oudesluijs, Gretel; van de Laar, Ingrid M B M; Martens, Liesbeth (2013-09). ”Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings” (på engelska). European Journal of Human Genetics 21 (9): sid. 936–942. doi:10.1038/ejhg.2012.285. ISSN 1018-4813. https://www.nature.com/articles/ejhg2012285. Läst 20 maj 2024.
Baldo, Francesco; Fachin, Alice; Da Re, Beatrice; Rubinato, Elisa; Bobbo, Marco; Barbi, Egidio (2022-12-24). ”New insights on Noonan syndrome’s clinical phenotype: a single center retrospective study” (på engelska). BMC Pediatrics 22 (1). doi:10.1186/s12887-022-03804-2. ISSN 1471-2431. https://bmcpediatr.biomedcentral.com/articles/10.1186/s12887-022-03804-2. Läst 20 maj 2024.
Tartaglia, Marco; Gelb, Bruce D.; Zenker, Martin (2011-02). ”Noonan syndrome and clinically related disorders” (på engelska). Best Practice & Research Clinical Endocrinology & Metabolism 25 (1): sid. 161–179. doi:10.1016/j.beem.2010.09.002. https://linkinghub.elsevier.com/retrieve/pii/S1521690X1000117X. Läst 20 maj 2024.
Zenker, Martin; Edouard, Thomas; Blair, Joanne C; Cappa, Marco (2022-12). ”Noonan syndrome: improving recognition and diagnosis” (på engelska). Archives of Disease in Childhood 107 (12): sid. 1073–1078. doi:10.1136/archdischild-2021-322858. ISSN 0003-9888. https://adc.bmj.com/lookup/doi/10.1136/archdischild-2021-322858. Läst 20 maj 2024.
García-Miñaúr, Sixto; Burkitt-Wright, Emma; Verloes, Alain; Shaikh, Guftar; Lebl, Jan; Östman-Smith, Ingegerd (2022-01). ”European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe” (på engelska). European Journal of Medical Genetics 65 (1): sid. 104371. doi:10.1016/j.ejmg.2021.104371. https://linkinghub.elsevier.com/retrieve/pii/S1769721221002378. Läst 20 maj 2024.
Roberts, Amy E; Allanson, Judith E; Tartaglia, Marco; Gelb, Bruce D (2013-01). ”Noonan syndrome”. The Lancet 381 (9863): sid. 333–342. doi:10.1016/s0140-6736(12)61023-x. ISSN 0140-6736. PMID 23312968. PMC: PMC4267483. https://doi.org/10.1016/S0140-6736(12)61023-X. Läst 16 maj 2024.
Mittal, Rahul; Kodiyan, Joyson; Gerring, Robert; Mathee, Kalai; Li, Jian-Dong; Grati, M’hamed (2014-12). ”Role of innate immunity in the pathogenesis of otitis media”. International Journal of Infectious Diseases 29: sid. 259–267. doi:10.1016/j.ijid.2014.10.015. ISSN 1201-9712. PMID 25447732. PMC: PMC4310697. https://doi.org/10.1016/j.ijid.2014.10.015. Läst 16 maj 2024.

doi.org

Roberts, Amy E; Allanson, Judith E; Tartaglia, Marco; Gelb, Bruce D (2013-01). ”Noonan syndrome”. The Lancet 381 (9863): sid. 333–342. doi:10.1016/s0140-6736(12)61023-x. ISSN 0140-6736. PMID 23312968. PMC: PMC4267483. https://doi.org/10.1016/S0140-6736(12)61023-X. Läst 16 maj 2024.
Mittal, Rahul; Kodiyan, Joyson; Gerring, Robert; Mathee, Kalai; Li, Jian-Dong; Grati, M’hamed (2014-12). ”Role of innate immunity in the pathogenesis of otitis media”. International Journal of Infectious Diseases 29: sid. 259–267. doi:10.1016/j.ijid.2014.10.015. ISSN 1201-9712. PMID 25447732. PMC: PMC4310697. https://doi.org/10.1016/j.ijid.2014.10.015. Läst 16 maj 2024.

elsevier.com

linkinghub.elsevier.com

Tartaglia, Marco; Gelb, Bruce D.; Zenker, Martin (2011-02). ”Noonan syndrome and clinically related disorders” (på engelska). Best Practice & Research Clinical Endocrinology & Metabolism 25 (1): sid. 161–179. doi:10.1016/j.beem.2010.09.002. https://linkinghub.elsevier.com/retrieve/pii/S1521690X1000117X. Läst 20 maj 2024.
García-Miñaúr, Sixto; Burkitt-Wright, Emma; Verloes, Alain; Shaikh, Guftar; Lebl, Jan; Östman-Smith, Ingegerd (2022-01). ”European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe” (på engelska). European Journal of Medical Genetics 65 (1): sid. 104371. doi:10.1016/j.ejmg.2021.104371. https://linkinghub.elsevier.com/retrieve/pii/S1769721221002378. Läst 20 maj 2024.

karger.com

Jorge, Alexander A.L.; Malaquias, Alexsandra C.; Arnhold, Ivo J.P.; Mendonca, Berenice B. (2009). ”Noonan Syndrome and Related Disorders: A Review of Clinical Features and Mutations in Genes of the RAS/MAPK Pathway” (på engelska). Hormone Research in Paediatrics 71 (4): sid. 185–193. doi:10.1159/000201106. ISSN 1663-2818. https://karger.com/HRE/article/doi/10.1159/000201106. Läst 19 maj 2024.

medlineplus.gov

”Noonan syndrome: MedlinePlus Genetics” (på engelska). medlineplus.gov. https://medlineplus.gov/genetics/condition/noonan-syndrome/. Läst 19 maj 2024.

nature.com

Croonen, Ellen A; Nillesen, Willy M; Stuurman, Kyra E; Oudesluijs, Gretel; van de Laar, Ingrid M B M; Martens, Liesbeth (2013-09). ”Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings” (på engelska). European Journal of Human Genetics 21 (9): sid. 936–942. doi:10.1038/ejhg.2012.285. ISSN 1018-4813. https://www.nature.com/articles/ejhg2012285. Läst 20 maj 2024.

nih.gov

ncbi.nlm.nih.gov

Allanson, Judith E. (1993). Roberta A. Pagon, Margaret P. Adam, Holly H. Ardinger, Stephanie E. Wallace, Anne Amemiya, Lora JH Bean, Thomas D. Bird, Nikki Ledbetter. red. GeneReviews(®). University of Washington, Seattle. http://www.ncbi.nlm.nih.gov/books/NBK1124/. Läst 20 maj 2017
Roberts, Amy E; Allanson, Judith E; Tartaglia, Marco; Gelb, Bruce D (2013-01). ”Noonan syndrome”. The Lancet 381 (9863): sid. 333–342. doi:10.1016/s0140-6736(12)61023-x. ISSN 0140-6736. PMID 23312968. PMC: PMC4267483. https://doi.org/10.1016/S0140-6736(12)61023-X. Läst 16 maj 2024.
Mittal, Rahul; Kodiyan, Joyson; Gerring, Robert; Mathee, Kalai; Li, Jian-Dong; Grati, M’hamed (2014-12). ”Role of innate immunity in the pathogenesis of otitis media”. International Journal of Infectious Diseases 29: sid. 259–267. doi:10.1016/j.ijid.2014.10.015. ISSN 1201-9712. PMID 25447732. PMC: PMC4310697. https://doi.org/10.1016/j.ijid.2014.10.015. Läst 16 maj 2024.

noonan.nu

”Home”. svenskanoonan. https://www.noonan.nu/. Läst 20 maj 2024.

rarediseases.org

”Noonan Syndrome - Symptoms, Causes, Treatment | NORD” (på amerikansk engelska). rarediseases.org. https://rarediseases.org/rare-diseases/noonan-syndrome/. Läst 20 maj 2024.

socialstyrelsen.se

”Noonans syndrom”. Socialstyrelsen. 5 november 2023. https://www.socialstyrelsen.se/kunskapsstod-och-regler/omraden/sallsynta-halsotillstand/noonans-syndrom/. Läst 19 maj 2024.

worldcat.org

Jorge, Alexander A.L.; Malaquias, Alexsandra C.; Arnhold, Ivo J.P.; Mendonca, Berenice B. (2009). ”Noonan Syndrome and Related Disorders: A Review of Clinical Features and Mutations in Genes of the RAS/MAPK Pathway” (på engelska). Hormone Research in Paediatrics 71 (4): sid. 185–193. doi:10.1159/000201106. ISSN 1663-2818. https://karger.com/HRE/article/doi/10.1159/000201106. Läst 19 maj 2024.
Croonen, Ellen A; Nillesen, Willy M; Stuurman, Kyra E; Oudesluijs, Gretel; van de Laar, Ingrid M B M; Martens, Liesbeth (2013-09). ”Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings” (på engelska). European Journal of Human Genetics 21 (9): sid. 936–942. doi:10.1038/ejhg.2012.285. ISSN 1018-4813. https://www.nature.com/articles/ejhg2012285. Läst 20 maj 2024.
Baldo, Francesco; Fachin, Alice; Da Re, Beatrice; Rubinato, Elisa; Bobbo, Marco; Barbi, Egidio (2022-12-24). ”New insights on Noonan syndrome’s clinical phenotype: a single center retrospective study” (på engelska). BMC Pediatrics 22 (1). doi:10.1186/s12887-022-03804-2. ISSN 1471-2431. https://bmcpediatr.biomedcentral.com/articles/10.1186/s12887-022-03804-2. Läst 20 maj 2024.
Zenker, Martin; Edouard, Thomas; Blair, Joanne C; Cappa, Marco (2022-12). ”Noonan syndrome: improving recognition and diagnosis” (på engelska). Archives of Disease in Childhood 107 (12): sid. 1073–1078. doi:10.1136/archdischild-2021-322858. ISSN 0003-9888. https://adc.bmj.com/lookup/doi/10.1136/archdischild-2021-322858. Läst 20 maj 2024.
Roberts, Amy E; Allanson, Judith E; Tartaglia, Marco; Gelb, Bruce D (2013-01). ”Noonan syndrome”. The Lancet 381 (9863): sid. 333–342. doi:10.1016/s0140-6736(12)61023-x. ISSN 0140-6736. PMID 23312968. PMC: PMC4267483. https://doi.org/10.1016/S0140-6736(12)61023-X. Läst 16 maj 2024.
Mittal, Rahul; Kodiyan, Joyson; Gerring, Robert; Mathee, Kalai; Li, Jian-Dong; Grati, M’hamed (2014-12). ”Role of innate immunity in the pathogenesis of otitis media”. International Journal of Infectious Diseases 29: sid. 259–267. doi:10.1016/j.ijid.2014.10.015. ISSN 1201-9712. PMID 25447732. PMC: PMC4310697. https://doi.org/10.1016/j.ijid.2014.10.015. Läst 16 maj 2024.