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Pituitary growth hormone insufficiency associated with cleft lip and palate. An embryonal developmental defect.

作者信息

Laron Z, Taube E, Kaplan I

出版信息

Helv Paediatr Acta. 1969 Dec;24(6):576-81.

PMID:5370797
Abstract
摘要

相似文献

1
Pituitary growth hormone insufficiency associated with cleft lip and palate. An embryonal developmental defect.与唇腭裂相关的垂体生长激素分泌不足。一种胚胎发育缺陷。
Helv Paediatr Acta. 1969 Dec;24(6):576-81.
2
[Pituitary dwarfism in cleft lip and cleft palate. Clinical case].[唇腭裂伴垂体性侏儒症。临床病例]
Minerva Pediatr. 1978 Jul 31;30(14):1163-6.
3
[Growth and growth hormone in children with congenital lip and palatal clefts].
Klin Padiatr. 1984 Sep-Oct;196(5):304-6. doi: 10.1055/s-2008-1034084.
4
Parental age and incidence of cleft lip and cleft palate anomalies.父母年龄与唇腭裂畸形的发生率
Acta Anthropogenet. 1984;8(3-4):231-5.
5
[Radio-immunologic determination of the human plasma growth hormone (S.T.H.). Contribution of the stimulation tests by arginine and insulin in the delimitation of a pituitary insufficiency].
Pathol Biol (Paris). 1970 Mar;18(5):241-53.
6
A comparison of the effects of insulin and pyrogen as stimuli to growth hormone release in man.胰岛素与热原作为人体生长激素释放刺激物的效果比较。
Johns Hopkins Med J. 1968 Mar;122(3):154-9.
7
The incidence of cleft lip and palate in Nigeria.尼日利亚唇腭裂的发病率。
Cleft Palate J. 1982 Jul;19(3):201-5.
8
[The causes of cleft palate and cleft lip].[腭裂和唇裂的病因]
Stomatol Vjesn. 1985;14(3-4):129-32.
9
Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24).一名26岁男性，因新发不平衡易位t(1;12)(q24;q24)导致生长激素缺乏未经治疗，身材极矮，伴有骨骼发育异常、唇腭裂和严重智力障碍。
Eur J Med Genet. 2007 Nov-Dec;50(6):455-64. doi: 10.1016/j.ejmg.2007.06.004. Epub 2007 Jul 20.
10
[Statistical interpretation of tests of the stimulation of secretion of growth-hormone by insulin and arginine].[胰岛素和精氨酸刺激生长激素分泌试验的统计学解释]
Arch Fr Pediatr. 1971 May;28(5):505-20.

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Genetic requirement for in vertebrate pituitary morphogenesis.脊椎动物垂体形态发生中的遗传需求。
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2
Morphological Variations and Anomalies of the Sella Turcica on Lateral Cephalograms of Cleft-Palate-Only (CPO) Patients.单纯腭裂（CPO）患者头颅侧位片上蝶鞍的形态变异与异常
Diagnostics (Basel). 2023 Jul 27;13(15):2510. doi: 10.3390/diagnostics13152510.
3
Cone-beam computed tomographic comparison of chin symphysis bone particles and allograft versus iliac crest bone graft alone for reconstruction of alveolar bone defects in cleft patients.
锥形束计算机断层扫描比较颏联合骨颗粒与同种异体骨联合自体髂骨移植与单纯自体髂骨移植用于腭裂患者牙槽骨缺损重建的效果
J Korean Assoc Oral Maxillofac Surg. 2022 Apr 30;48(2):85-93. doi: 10.5125/jkaoms.2022.48.2.85.
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Common basis for orofacial clefting and cortical interneuronopathy.口面裂和皮质中间神经元病的共同基础。
Transl Psychiatry. 2018 Jan 10;8(1):8. doi: 10.1038/s41398-017-0057-7.
5
Cleft lip and palate and related factors: A 10 years study in university hospitalised patients at Mashhad--Iran.唇腭裂及相关因素：对伊朗马什哈德大学附属医院住院患者的10年研究
Afr J Paediatr Surg. 2015 Oct-Dec;12(4):286-90. doi: 10.4103/0189-6725.172576.
6
Characterization of subtle brain abnormalities in a mouse model of Hedgehog pathway antagonist-induced cleft lip and palate.Hedgehog信号通路拮抗剂诱导的唇腭裂小鼠模型中细微脑异常的特征分析
PLoS One. 2014 Jul 21;9(7):e102603. doi: 10.1371/journal.pone.0102603. eCollection 2014.
7
Height, BMI, and pituitary volume in individuals with and without isolated cleft lip and/or palate.单纯唇裂和/或腭裂患者与非单纯唇裂和/或腭裂患者的身高、体重指数和垂体体积。
Pediatr Res. 2012 May;71(5):612-8. doi: 10.1038/pr.2012.12. Epub 2012 Feb 9.
8
Cleft lip and palate results from Hedgehog signaling antagonism in the mouse: Phenotypic characterization and clinical implications.小鼠中刺猬信号通路拮抗作用导致唇腭裂：表型特征及临床意义
Birth Defects Res A Clin Mol Teratol. 2010 Apr;88(4):232-40. doi: 10.1002/bdra.20656.
9
Longitudinal study of growth of children with unilateral cleft-lip palate from birth to two years of age.单侧唇腭裂患儿从出生到两岁生长情况的纵向研究。
Cleft Palate Craniofac J. 2009 Nov;46(6):603-9. doi: 10.1597/08-105.1. Epub 2009 May 16.
10
Hypopituitarism associated with transsphenoidal meningoencephalocele.与经蝶窦脑膜脑膨出相关的垂体功能减退症。
Eur J Pediatr. 1982 Sep;139(1):81-4. doi: 10.1007/BF00442087.