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Leonie A Menke

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Hormone Research in Paediatrics|November 6, 2010
Comments on 'Prospective study confirms oxandrolone-associated improvement in height in growth hormone-treated adolescent girls with Turner syndrome' by Zeger et al., pp. 39-47, this issueLeonie A Menke, Theo C J Sas, Jan M Wit
Hormone Research in Paediatrics|July 15, 2019
Towards a Rational and Efficient Diagnostic Approach in Children Referred for Tall Stature and/or Accelerated Growth to the General PaediatricianPeter Lauffer, Gerdine A Kamp, Leonie A Menke, et al.
Journal of Child Neurology|September 15, 2016
Recurrent GNAO1 Mutations Associated With Developmental Delay and a Movement DisorderLeonie A Menke, Marc Engelen, Mariel Alders, et al.
BMC Pediatrics|July 31, 2019
Marfan syndrome in childhood: parents' perspectives of the impact on daily functioning of children, parents and family; a qualitative studyJessica Warnink-Kavelaars, Anita Beelen, Sarah Dekker, et al.
American Journal of Medical Genetics. Part A|February 22, 2023
Severe early-onset overgrowth in a case of pseudohypoparathyroidism type 1b, caused by STX16 deletionNiels Vos, Leonie A Menke, Christiaan F Mooij, et al.
American Journal of Medical Genetics. Part A|December 13, 2022
Fatal gastrointestinal complications in Pitt-Hopkins syndromeIlan J N Koppen, Leonie A Menke, Wytske M Westra, et al.
Journal of Intellectual Disability Research : JIDR|January 28, 2026
What Matters Most? Developing a Core Patient Reported Outcome Set for Individuals With Genetic Intellectual Disabilities: An International Delphi StudyNadia Y van Silfhout, Maud M van Muilekom, Leonie A Menke, et al.
American Journal of Medical Genetics. Part A|October 9, 2020
Parenting a child with Marfan syndrome: Distress and everyday problemsJessica Warnink-Kavelaars, Hedy A van Oers, Lotte Haverman, et al.
European Journal of Medical Genetics|June 13, 2008
Ectrodactyly with fibular aplasia: a separate entity?Leonie A Menke, Emilia K Bijlsma, Anthonie J van Essen, et al.
American Journal of Medical Genetics. Part A|February 13, 2008
Congenital heart defects in spinal muscular atrophy type I: a clinical report of two siblings and a review of the literatureLeonie A Menke, Bwee Tien Poll-The, Sally-Ann Clur, et al.
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Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Hormone Research in Paediatrics|November 6, 2010
Comments on 'Prospective study confirms oxandrolone-associated improvement in height in growth hormone-treated adolescent girls with Turner syndrome' by Zeger et al., pp. 39-47, this issueLeonie A Menke, Theo C J Sas, Jan M Wit
Hormone Research in Paediatrics|July 15, 2019
Towards a Rational and Efficient Diagnostic Approach in Children Referred for Tall Stature and/or Accelerated Growth to the General PaediatricianPeter Lauffer, Gerdine A Kamp, Leonie A Menke, et al.
Journal of Child Neurology|September 15, 2016
Recurrent GNAO1 Mutations Associated With Developmental Delay and a Movement DisorderLeonie A Menke, Marc Engelen, Mariel Alders, et al.
BMC Pediatrics|July 31, 2019
Marfan syndrome in childhood: parents' perspectives of the impact on daily functioning of children, parents and family; a qualitative studyJessica Warnink-Kavelaars, Anita Beelen, Sarah Dekker, et al.
American Journal of Medical Genetics. Part A|February 22, 2023
Severe early-onset overgrowth in a case of pseudohypoparathyroidism type 1b, caused by STX16 deletionNiels Vos, Leonie A Menke, Christiaan F Mooij, et al.
American Journal of Medical Genetics. Part A|December 13, 2022
Fatal gastrointestinal complications in Pitt-Hopkins syndromeIlan J N Koppen, Leonie A Menke, Wytske M Westra, et al.
Journal of Intellectual Disability Research : JIDR|January 28, 2026
What Matters Most? Developing a Core Patient Reported Outcome Set for Individuals With Genetic Intellectual Disabilities: An International Delphi StudyNadia Y van Silfhout, Maud M van Muilekom, Leonie A Menke, et al.
American Journal of Medical Genetics. Part A|October 9, 2020
Parenting a child with Marfan syndrome: Distress and everyday problemsJessica Warnink-Kavelaars, Hedy A van Oers, Lotte Haverman, et al.
European Journal of Medical Genetics|June 13, 2008
Ectrodactyly with fibular aplasia: a separate entity?Leonie A Menke, Emilia K Bijlsma, Anthonie J van Essen, et al.
American Journal of Medical Genetics. Part A|February 13, 2008
Congenital heart defects in spinal muscular atrophy type I: a clinical report of two siblings and a review of the literatureLeonie A Menke, Bwee Tien Poll-The, Sally-Ann Clur, et al.
Pageof 5