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3-M syndrome: description of six new patients with review of the literature.
van der Wal G, Otten BJ, Brunner HG, van der Burgt I. van der Wal G, et al. Among authors: otten bj. Clin Dysmorphol. 2001 Oct;10(4):241-52. doi: 10.1097/00019605-200110000-00002. Clin Dysmorphol. 2001. PMID: 11665997 Review.
[Growth hormone therapy in dysmorphic syndromes and chronic disease].
Otten BJ, Wit JM. Otten BJ, et al. Tijdschr Kindergeneeskd. 1992 Oct;60(5):183-91. Tijdschr Kindergeneeskd. 1992. PMID: 1448809 Review. Dutch.
Influence of treatment modalities on prepubertal growth in children with acute lymphoblastic leukemia.
Groot-Loonen JJ, Otten BJ, van't Hof MA, Lippens RJ, Stoelinga GB. Groot-Loonen JJ, et al. Among authors: otten bj. Pediatr Hematol Oncol. 1995 Jul-Aug;12(4):343-53. doi: 10.3109/08880019509029584. Pediatr Hematol Oncol. 1995. PMID: 7577386 Clinical Trial.
Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation.
Kotzot D, Schmitt S, Bernasconi F, Robinson WP, Lurie IW, Ilyina H, Méhes K, Hamel BC, Otten BJ, Hergersberg M, et al. Kotzot D, et al. Among authors: otten bj. Hum Mol Genet. 1995 Apr;4(4):583-7. doi: 10.1093/hmg/4.4.583. Hum Mol Genet. 1995. PMID: 7633407
Long-term results of growth hormone therapy in children with short stature, subnormal growth rate and normal growth hormone response to secretagogues. Dutch Growth Hormone Working Group.
Wit JM, Boersma B, de Muinck Keizer-Schrama SM, Nienhuis HE, Oostdijk W, Otten BJ, Delemarre-Van de Waal HA, Reeser M, Waelkens JJ, Rikken B, et al. Wit JM, et al. Among authors: otten bj. Clin Endocrinol (Oxf). 1995 Apr;42(4):365-72. doi: 10.1111/j.1365-2265.1995.tb02644.x. Clin Endocrinol (Oxf). 1995. PMID: 7750190 Clinical Trial.
Antibody deficiency and isolated growth hormone deficiency in a girl with Mulibrey nanism.
Haraldsson A, van der Burgt CJ, Weemaes CM, Otten B, Bakkeren JA, Stoelinga GB. Haraldsson A, et al. Eur J Pediatr. 1993 Jun;152(6):509-12. doi: 10.1007/BF01955061. Eur J Pediatr. 1993. PMID: 8335020
Catch-up growth after prolonged hypothyroidism.
Boersma B, Otten BJ, Stoelinga GB, Wit JM. Boersma B, et al. Among authors: otten bj. Eur J Pediatr. 1996 May;155(5):362-7. doi: 10.1007/BF01955262. Eur J Pediatr. 1996. PMID: 8741031
Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findings.
Hamel BC, Smits AP, Otten BJ, van den Helm B, Ropers HH, Mariman EC. Hamel BC, et al. Among authors: otten bj. Am J Med Genet. 1996 Jul 12;64(1):35-41. doi: 10.1002/(SICI)1096-8628(19960712)64:1<35::AID-AJMG5>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8826446
Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndrome.
Cremers WR, Bolder C, Admiraal RJ, Everett LA, Joosten FB, van Hauwe P, Green ED, Otten BJ. Cremers WR, et al. Among authors: otten bj. Arch Otolaryngol Head Neck Surg. 1998 May;124(5):501-5. doi: 10.1001/archotol.124.5.501. Arch Otolaryngol Head Neck Surg. 1998. PMID: 9604973
Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome.
Cremers CW, Admiraal RJ, Huygen PL, Bolder C, Everett LA, Joosten FB, Green ED, van Camp G, Otten BJ. Cremers CW, et al. Among authors: otten bj. Int J Pediatr Otorhinolaryngol. 1998 Oct 2;45(2):113-23. doi: 10.1016/s0165-5876(98)00123-2. Int J Pediatr Otorhinolaryngol. 1998. PMID: 9849679
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