Michael Hauschild

Publications | Phd and Masters theses

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49 publications

2023 | 2022 | 2021 | 2020 | 2019 | 2018 | 2017 | 2016 | 2015 | 2014 | 2013 | 2012 | 2011 | 2010 | 2009 | 2007 | 2006 | 2000 |
2023
Glucose variability in 6-12-month-old healthy infants.
Hauschild M., Monnard C., Eldridge A.L., Antoniou M.C., Bouthors T., Hansen E., Dwyer A.A., Rytz A., Darimont C., 2023/07. Frontiers in nutrition, 10 p. 1128389. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_BB5F57F37426]
 
Diabète monogénique : pionnier dans la prise en charge par la médecine de précision [Monogenic diabetes : a pioneer in precision medicine management]
Iafrate-Luterbacher F., Dirlewanger M., Hauschild M., Schwitzgebel V.M., Busiah K., 2023/02/22. Revue medicale suisse, 19 (815) pp. 362-367. Peer-reviewed.
[URN][DOI][Pmid][serval:BIB_A5446557AAD2]
 
Obésité infantile : nouveautés thérapeutiques ciblées [Obesity in infancy: new precision treatment]
Ruiz I., Bouthors T., Borloz S., Hauschild M., Maggio A., Schwitzgebel V.M., 2023/02/22. Revue medicale suisse, 19 (815) pp. 374-379. Peer-reviewed.
[URN][DOI][Pmid][serval:BIB_2C297F4168CD]
Turner syndrome: skin, liver, eyes, dental and ENT evaluation should be improved.
Lam J., Stoppa-Vaucher S., Antoniou M.C., Bouthors T., Ruiz I., Sekarski N., Rutz T., Fries S., Binz P.A., Bütschi F.N. et al., 2023. Frontiers in endocrinology, 14 p. 1190670. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_F5565E7EFFFF]
2022
High Prevalence of Hypovitaminosis D in Adolescents Attending a Reference Centre for the Treatment of Obesity in Switzerland.
Patriota P., Borloz S., Ruiz I., Bouthors T., Rezzi S., Marques-Vidal P., Hauschild M., 2022/10/06. Children, 9 (10) p. 1527. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_C5DF8A37580B]
Nouvelle technologie de gestion du diabète: apprendre ensemble et en situation [New technology of diabetes management: learning together and in situation]
Pralong M., Danesi G., Panese F., Burnand B., Hauschild M., Grossen M., 2022/09/21. Revue medicale suisse, 18 (796) pp. 1767-1769. Peer-reviewed.
[URN][DOI][Pmid][serval:BIB_39E1898A11E6]
Navigating Disrupted Puberty: Development and Evaluation of a Mobile-Health Transition Passport for Klinefelter Syndrome.
Dwyer A.A., Héritier V., Llahana S., Edelman L., Papadakis G.E., Vaucher L., Pitteloud N., Hauschild M., 2022. Frontiers in endocrinology, 13 p. 909830. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_3938769A5C18]
2021
Learning to manage diabetes using a flash glucose monitoring device at a summer camp: A collective appropriation process
Danesi Giada, Pralong Mélody, Grossen Michèle, Panese Francesco, Hauschild Michael, Burnand Bernard, 2021/12. Learning, Culture and Social Interaction, 31 p. 100570. Peer-reviewed.
[URN][DOI][WoS][serval:BIB_B96CBA88ED58]
Correction to: Elevated lactate in Mauriac syndrome: still a mystery.
Touilloux B., Lu H., Campos-Xavier B., Superti-Furga A., Hauschild M., Bouthors T., Tran C., 2021/09/30. BMC endocrine disorders, 21 (1) p. 194. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_C20E707E2A26]
 
Elevated lactate in Mauriac syndrome: still a mystery.
Touilloux B., Lu H., Campos-Xavier B., Superti-Furga A., Hauschild M., Bouthors T., Tran C., 2021/08/21. BMC endocrine disorders, 21 (1) p. 172. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_8EAC9E849686]
 
Health behaviour of women with Turner Syndrome.
Santi M., Flück C.E., Hauschild M., Kuhlmann B., Kuehni C.E., Sommer G., 2021/08. Acta paediatrica, 110 (8) pp. 2424-2429. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_F449104A4325]
Congenital hyperinsulinism: 2 case reports with different rare variants in ABCC8.
Mouron-Hryciuk J., Stoppa-Vaucher S., Busiah K., Bouthors T., Antoniou M.C., Jacot E., Brusgaard K., Christesen H.T., Hussain K., Dwyer A. et al., 2021/03. Annals of pediatric endocrinology & metabolism, 26 (1) pp. 60-65. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_91DFF95FA52E]
 
Insulin-like Growth Factor 1, but Not Insulin-Like Growth Factor-Binding Protein 3, Predicts Central Precocious Puberty in Girls 6-8 Years Old: A Retrospective Study.
Escagedo P.D., Deal C.L., Dwyer A.A., Hauschild M., 2021. Hormone research in paediatrics, 94 (1-2) pp. 44-51. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_C5C8256A98DF]
2020
Syndrome des ovaires polykystiques chez l’adolescente diabétique ou obèse [Polycystic ovary syndrome in obese or type 1 diabetic (T1D) adolescent girls]
Bouthors T., Elowe-Gruau É., Antoniou M.C., Hryciuk J., Stoppa-Vaucher S., Ruiz Arana I.L., Diserens C., Busiah K., Hauschild M., 2020/10/14. Revue medicale suisse, 16 (710) pp. 1941-1944. Peer-reviewed.
[URN][DOI][Pmid][serval:BIB_60A93331D71E]
Non-invasive assessment of coronary endothelial function in children and adolescents with type 1 diabetes mellitus using isometric handgrip exercise-MRI: A feasibility study.
Zwingli G., Yerly J., Mivelaz Y., Stoppa-Vaucher S., Dwyer A.A., Pitteloud N., Stuber M., Hauschild M., 2020. PloS one, 15 (2) pp. e0228569. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_FA9042213A7F]
2019
A novel CHD7 mutation in an adolescent presenting with growth and pubertal delay.
Antoniou M.C., Bouthors T., Xu C., Phan-Hug F., Elowe-Gruau E., Stoppa-Vaucher S., Sloot A.V., Acierno J., Cassatella D., Richard C. et al., 2019/03. Annals of pediatric endocrinology & metabolism, 24 (1) pp. 49-54. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_4F2DE07B705C]
2018
 
Accuracy, satisfaction and usability of a flash glucose monitoring system among children and adolescents with type 1 diabetes attending a summer camp.
Hansen E.A., Klee P., Dirlewanger M., Bouthors T., Elowe-Gruau E., Stoppa-Vaucher S., Phan-Hug F., Antoniou M.C., Pasquier J., Dwyer A.A. et al., 2018/11. Pediatric diabetes, 19 (7) pp. 1276-1284. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_E4CA6EAA378C]
 
Kinder und Jugendliche mit Varianten in der Geschlechtsentwicklung - Enfants et adolescents avec variations du développement sexuel
Sommer Grit, Konrad Daniel, Kuhlmann Beatrice, L'Allemand Dagmar, Phan-Hug Franziska, Hauschild Michael, Schwitzgebel Valerie, Tonella Paolo, Hess Melanie, Zumsteg Urs et al., 2018/10/17. Swiss Medical Forum ‒ Schweizerisches Medizin-Forum.
[DOI][serval:BIB_E0FA87E23962]
 
Perturbateurs endocriniens chez l’enfant
Bouthors Thérèse, Hauschild Michael, 2018/09/25. Paediatrica, 29 (4) pp. 27-31.
[serval:BIB_03876F4C9B38]
 
Evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants
Xu Cheng, Cassatella Daniele, van der Sloot Almer M, Quinton Richard, Hauschild Michael, De Geyter Christian, Flück Christa, Feller Katrin, Bartholdi Deborah, Nemeth Attila et al., 2018/08. Genetics in Medicine, 20 (8) pp. 872-881.
[DOI][WoS][Pmid][serval:BIB_3F5E9AC47FE9]
Evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants.
Xu C., Cassatella D., van der Sloot A.M., Quinton R., Hauschild M., De Geyter C., Flück C., Feller K., Bartholdi D., Nemeth A. et al., 2018/08. Genetics in medicine, 20 (8) pp. 872-881. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_88754A56C4C4]
 
Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures
Cassatella Daniele, Howard Sasha R, Acierno James S, Xu Cheng, Papadakis Georgios E, Santoni Federico A, Dwyer Andrew A, Santini Sara, Sykiotis Gerasimos P, Chambion Caroline et al., 2018/04. European Journal of Endocrinology, 178 (4) pp. 377-388.
[DOI][WoS][Pmid][serval:BIB_334A063EB536]
Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures.
Cassatella D., Howard S.R., Acierno J.S., Xu C., Papadakis G.E., Santoni F.A., Dwyer A.A., Santini S., Sykiotis G.P., Chambion C. et al., 2018/04. European journal of endocrinology, 178 (4) pp. 377-388. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_92D278111021]
 
Défis de la transition de l’adolescent obèse aux soins adultes [Challenges of the transition for obese teenager towards adult care]
Roth Pressl-Wenger A., Clarisse M., Hauschild M., Borloz S., Bouthors T., Favre L., 2018/03/21. Revue medicale suisse, 14 (599) pp. 615-619. Peer-reviewed.
[Pmid][serval:BIB_D745D1C689A3]
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.
Bouilly J., Messina A., Papadakis G., Cassatella D., Xu C., Acierno J.S., Tata B., Sykiotis G., Santini S., Sidis Y. et al., 2018/01/15. Human molecular genetics, 27 (2) pp. 359-372. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_E34B12561F91]
 
Patient Perspectives on Nurse-led Consultations Within a Pilot Structured Transition Program for Young Adults Moving From an Academic Tertiary Setting to Community-based Type 1 Diabetes Care.
Zoni S., Verga M.E., Hauschild M., Aquarone-Vaucher M.P., Gyuriga T., Ramelet A.S., Dwyer A.A., 2018. Journal of pediatric nursing, 38 pp. 99-105. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_140565A7E10A]
2017
Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism.
COST Action BM1105, Badiu C., Bonomi M., Borshchevsky I., Cools M., Craen M., Ghervan C., Hauschild M., Hershkovitz E., Hrabovszky E. et al., 2017/03/20. Orphanet journal of rare diseases, 12 (1) p. 57. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_ADF811744A1B]
 
Transition from paediatric to adult care: what makes it easier for parents?
Suris J.C., Larbre J.P., Hofer M., Hauschild M., Barrense-Dias Y., Berchtold A., Akre C., 2017/01. Child, 43 (1) pp. 152-155. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_A522D678E5AC]
2016
 
Accueil des jeunes diabétiques à l’école- Stratégies et recommandations de la SSEDP
Hauschild Michael, Bachmann Sara , Mullis Primus , Gozzi Graf Tiziana , Tonella Paolo , Kuhlmann Beatrice , Steigert Michael , Lang-Muritano Mariarosaria, Wildi Stefanie, Geiser Corinne et al., 2016/06/29. Paediatrica, 27 (1) pp. 18-25.
[serval:BIB_3B2BB4E34231]
2015
 
Disseminated Cutaneous Mycobacterium chelonae Infection in a 9.5-Year-Old Girl with Diabetes
PA Crisinel, K Jaton, O Abbo, S Hiroz, M Hauschild, 2015/12. Journal of Case Reports and Studies, 3 (6).
[DOI][serval:BIB_4E9BEF44B3AA]
Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations.
Villanueva C., Jacobson-Dickman E., Xu C., Manouvrier S., Dwyer A.A., Sykiotis G.P., Beenken A., Liu Y., Tommiska J., Hu Y. et al., 2015/11. Genetics In Medicine : Official Journal of the American College of Medical Genetics, 17 (8) pp. 651-659. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_DD27A8DA5823]
 
Diabetes and immune thrombocytopenic purpura: a new association with good response to anti-CD20 therapy.
von Laer Tschudin L., Schwitzgebel V.M., von Scheven-Gête A., Blouin J.L., Hofer M., Hauschild M., Ansari M., Stoppa-Vaucher S., Phan-Hug F., 2015. Pediatric Diabetes, 16 (2) pp. 138-145. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_F096E98DD4AF]
Health-Related Quality of Life of Young Adults Treated with Recombinant Human Growth Hormone during Childhood.
Sommer G., Gianinazzi M.E., Kuonen R., Bohlius J., l'Allemand D., Hauschild M., Mullis P.E., Kuehni C.E., Swiss Society for Paediatric Endocrinology, Diabetology (SGPED), 2015. Plos One, 10 (10) pp. e0140944. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_4E537515F421]
 
Natural history of growth hormone deficiency in a pediatric cohort.
Deillon E., Hauschild M., Faouzi M., Stoppa-Vaucher S., Elowe-Gruau E., Dwyer A., Theintz G.E., Dubuis J.M., Mullis P.E., Pitteloud N. et al., 2015. Hormone Research In Pædiatrics, 83 (4) pp. 252-261. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_AF2E8B8BC454]
 
Transition en diabétologie [Transition in diabetology].
Hauschild M., Elowe-Gruau E., Dwyer A., Aquarone M.P., Unal S., Jornayvaz F.R., Perrenoud L., Gastaldi G., Castellsague M., Dirlewanger M. et al., 2015. Revue Médicale Suisse, 11 (462) pp. 450-2, 454-5.
[Pmid][serval:BIB_E2BECF473AA3]
 
TRANSITION IN ENDOCRINOLOGY: Hypogonadism in adolescence.
Dwyer A.A., Phan-Hug F., Hauschild M., Elowe-Gruau E., Pitteloud N., 2015. European Journal of Endocrinology, 173 (1) pp. R15-R24. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_8F5B9A78BBD8]
2014
 
Suivi et prise en charge des enfants nés petits pour l'âge gestationnel: aspects endo- crinologiques et métaboliques [Follow-up and management of children born small for gestational age a endocrine and metabolic aspects].
Elowe-Gruau E., Phan-Hug F., Stoppa-Vaucher S., Pitteloud N., Hauschild M., 2014. Revue Médicale Suisse, 10 (418) pp. 424, 426-424, 429.
[Pmid][serval:BIB_EF1588B137A7]
2013
 
Short stature, complex cardiac defects, and developmental delay associated with a de novo microduplication of chromosome 15q13.2q13
Hauschild M, Martinet D, Phan Hug F, Stoppa S, Cassatella D, Dwyer A, Pitteloud N, Addor MC, 2013. dans Congrès de la Société Suisse d'endocrinologie pédiatrique, Septembre 2013.
[serval:BIB_44463DC58A99]
2012
 
Concomitant blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and congenital adrenal hyperplasia (CAH) in a young girl
Decarli Diserens M, Addor MC, Stoppa S, Phan-Hug F, Pitteloud N, Hauschild M, 2012. dans Congrès de la Société Suisse de Pédiatrie, Lucerne 2012.
[serval:BIB_307DBF7093FF]
 
Prise en charge des jeunes patients avec endocrinopathies pediatriques chroniques: les défis d'une transition souvent difficile [Caring for patients with pediatric endocrinopathies and diabetes into adulthood: challenges of an often difficult transition].
Phan-Hug F., Hauschild M., Dwyer A., Pitteloud N., 2012. Revue Médicale Suisse, 8 (362) pp. 2170-2, 2174.
[Pmid][serval:BIB_60306F2F5A09]
 
Pédiatrie [Pediatrics].
Fischer C.J., Giannoni E., Truttmann A.C., Tolsa J.F., Chevallay M., El Ezzi O., Seneggen E., Hohlfeld J., de Buys Roessingh A., Pauchard J.Y. et al., 2012. Revue Médicale Suisse, 8 (323) pp. 51-56. Peer-reviewed.
[URN][Pmid][serval:BIB_09C64A04EE59]
2011
 
Diabète de l'enfant, de l'insulino- vers l'immunothérapie: une prise en charge globale du présent vers le futur [Current and future care for diabetes in children: from insulin to immunotherapy]
Dirlewanger M., Hauschild M., Phan-Hug F., Schwitzgebel V.M., 2011/02/23. Revue medicale suisse, 7 (283) pp. 430-436. Peer-reviewed.
[Pmid][serval:BIB_1EF8F44029E9]
2010
 
Idiopathic central diabetes insipidus in a premature newborn successfully treated by sublingual desmopressin
Bianchi Y El Faleh I Pastore Y Ecoffey M Laubscher B Hauschild M, 2010/05. dans Swiss Medwkly 2010:140 (Suppl. 180).
[serval:BIB_F10EABC9F225]
 
Failure to thrive in a girl born into a family affected by familial dysalbuminemic hyperthyroxinemia
Courvoisier M., von Scheven A., Vienny H., Zambelli P.Y., Hauschild M., 2010. pp. 22S-23S dans Joint annual meeting of the Swiss Society for Pediatrics and Swiss Society of Pediatric Pneumology, Swiss Medical Weekly. Peer-reviewed.
[WoS][serval:BIB_CD65DA182C06]
2009
 
Extreme self-monitoring, fear of hypoglycemia and obsessive-compulsive disorder in type 1 diabetes mellitus: when less is better
Hauschild Michael J., Merz Brigitte, Cuendet Sylvie, Moreillon Karine, Theintz Gerald E., 2009. p. 319 dans LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology in collaboration with APEG, APPES, JSPE and SLEP, Hormone Research. Peer-reviewed.
[WoS][serval:BIB_EA5A489576E1]
2007
 
Anemie chronique severe et anomalies endocrines chez l'enfant. [Severe chronic anemia and endocrine disorders in children]
Hauschild M., Theintz G., 2007/04. Revue Médicale Suisse, 3 (107) pp. 988-91.
[Pmid][serval:BIB_2CE3DACF5105]
 
Atypical presentation of Prader-Willi syndrome with cerebral venous thrombosis: association or fortuity?
Beretta L., Hauschild M., Jeannet P.Y., Addor M.C., Maeder P., Truttmann A.C., 2007. Neuropediatrics, 38 (4) pp. 204-206. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_033C89A8B682]
2006
 
Gesundheitsbezogene Lebensqualität von Geschwistern an Diabetes mellitus Typ 1 erkrankter Kinder und Jugendlicher
Gundlach S, Würz J, Schmutzer G, Hiermann P, Kapellen T, Galler A, Wudy S, Hauschild M, Kiess W, Brähler E, 2006/05. DMW - Deutsche Medizinische Wochenschrift, 131 (20) pp. 1143-1148.
[DOI][WoS][Pmid][serval:BIB_10A0AA414854]
2000
 
A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex I
Scharfe C., Hauschild M., Klopstock T., Janssen AJ, Heidemann PH, Meitinger T., Jaksch M., 2000/09/01. Journal of Medical Genetics, 37 (9) pp. 669-673.
[DOI][WoS][Pmid][serval:BIB_F5B596C42558]
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