841 results on '"Wit, Jan M"'
Search Results
2. Genetic findings in short Turkish children born to consanguineous parents
3. SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling
4. Digital Confessions: The Willingness to Disclose Intimate Information to a Chatbot and its Impact on Emotional Well-Being.
5. Disorders of IGFs and IGF-1R signaling pathways
6. Identification of novel genetic variants associated with short stature in a Baka Pygmies population
7. Perceived Discomfort Levels in Healthy Children Participating in Vaccine Research
8. Identification of novel genes including NAV2 associated with isolated tall stature
9. The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP
10. Screening for potential child maltreatment in parents of a newborn baby: The predictive validity of an Instrument for early identification of Parents At Risk for child Abuse and Neglect (IPARAN)
11. Growth Hormone-Releasing Hormone Receptor and Growth Hormone Gene Abnormalities
12. Long-term BMI and growth profiles in offspring of women with gestational diabetes
13. Atypical defects resulting in growth hormone insensitivity
14. Atypical STAT5B deficiency, severe short stature and mild immunodeficiency associated with a novel homozygous STAT5B Variant
15. Growth charts for Marfan syndrome in the Netherlands and analysis of genotype–phenotype relationships
16. Assessment of Nutritional Status in the Diagnostic Evaluation of the Child with Growth Failure.
17. A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High IGF-I Values at Transition to Adult Care.
18. Assessment of Nutritional Status in the Diagnostic Evaluation of the Child with Growth Failure
19. Mid-pregnancy, perinatal, and neonatal reproductive endocrinology: a prospective cohort study in twins and singleton control subjects
20. Novel approaches to short stature therapy
21. Regulating 'Higher Risk, No Direct Benefit' Studies with Children: Challenging the US Federal Regulations
22. Evidence-Based Guidelines for Growth Monitoring
23. Long-acting PEGylated growth hormone in children with idiopathic short stature: time to reconsider our diagnostic and treatment policy?
24. Vitamin D receptor polymorphisms and growth until adulthood after very premature birth
25. Growth charts for Marfan syndrome in the Netherlands and analysis of genotype–phenotype relationships
26. Differentiating the roles of STAT5B and STAT5A in human CD4+ T cells
27. The Effect of Early Catch-Up Growth on Health and Well-Being in Young Adults
28. Short and tall stature: a new paradigm emerges
29. The effect of family-based multidisciplinary cognitive behavioral treatment on health-related quality of life in childhood obesity
30. IGSF1 variants in boys with familial delayed puberty
31. Acceptable risks and burdens for children in research without direct benefit: a systematic analysis of the decisions made by the Dutch Central Committee
32. Ways to Improve the Diagnosis of Growth Hormone Deficiency
33. STAT5b deficiency: Lessons from STAT5b gene mutations
34. The Effect of Oxandrolone on Voice Frequency in Growth Hormone-Treated Girls With Turner Syndrome
35. Apc bridges Wnt/β-catenin and BMP signaling during osteoblast differentiation of KS483 cells
36. A Novel Method for Adult Height Prediction in Children With Idiopathic Short Stature Derived From a German-Dutch Cohort
37. Biallelic POC1A variants cause syndromic severe insulin resistance with muscle cramps
38. A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High IGF-I Values at Transition to Adult Care
39. Should Skeletal Maturation Be Manipulated for Extra Height Gain?
40. A Human Variant of Glucose-Regulated Protein 94 That Inefficiently Supports IGF Production
41. The effect of the weak androgen oxandrolone on psychological and behavioral characteristics in growth hormone-treated girls with Turner syndrome
42. Ways to Improve the Diagnosis of Growth Hormone Deficiency
43. Obituary: Dr. Marie-José Walenkamp (1966-2021)
44. An XRCC4 Splice Mutation Associated With Severe Short Stature, Gonadal Failure, and Early-Onset Metabolic Syndrome
45. PAPSS2 Deficiency Causes Androgen Excess via Impaired DHEA Sulfation—In Vitro and in Vivo Studies in a Family Harboring Two Novel PAPSS2 Mutations
46. WNT Signaling and Cartilage: Of Mice and Men
47. Discomfort in children undergoing unsedated MRI
48. Single gene mutations causing SGA
49. Antenatal Glucocorticoid Treatment and Polymorphisms of the Glucocorticoid and Mineralocorticoid Receptors are Associated with IQ and Behavior in Young Adults Born Very Preterm
50. Effects of individualized developmental care in a randomized trial of preterm infants <32 weeks
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