Binder G - Search Results

1

Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikely.

Eggermann K, Wollmann HA, Binder G, Kaiser P, Ranke MB, Eggermann T. Eggermann K, et al. Among authors: binder g. Ann Genet. 1999;42(2):117-21. Ann Genet. 1999. PMID: 10434128

2

Screening for growth hormone (GH) gene splice-site mutations in sporadic cases with severe isolated GH deficiency using ectopic transcript analysis.

Binder G, Ranke MB. Binder G, et al. J Clin Endocrinol Metab. 1995 Apr;80(4):1247-52. doi: 10.1210/jcem.80.4.7714096. J Clin Endocrinol Metab. 1995. PMID: 7714096

3

Nested polymerase chain reaction study of 53 cases with Turner's syndrome: is cytogenetically undetected Y mosaicism common?

Binder G, Koch A, Wajs E, Ranke MB. Binder G, et al. J Clin Endocrinol Metab. 1995 Dec;80(12):3532-6. doi: 10.1210/jcem.80.12.8530595. J Clin Endocrinol Metab. 1995. PMID: 8530595

4

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome.

Rao E, Weiss B, Fukami M, Rump A, Niesler B, Mertz A, Muroya K, Binder G, Kirsch S, Winkelmann M, Nordsiek G, Heinrich U, Breuning MH, Ranke MB, Rosenthal A, Ogata T, Rappold GA. Rao E, et al. Among authors: binder g. Nat Genet. 1997 May;16(1):54-63. doi: 10.1038/ng0597-54. Nat Genet. 1997. PMID: 9140395

5

Outcome in tall stature. Final height and psychological aspects in 220 patients with and without treatment.

Binder G, Grauer ML, Wehner AV, Wehner F, Ranke MB. Binder G, et al. Eur J Pediatr. 1997 Dec;156(12):905-10. doi: 10.1007/s004310050740. Eur J Pediatr. 1997. PMID: 9453370

6

De novo mutations of the growth hormone gene: an important cause of congenital isolated growth hormone deficiency?

Massa GG, Binder G, Oostdijk W, Ranke MB, Wit JM. Massa GG, et al. Among authors: binder g. Eur J Pediatr. 1998 Apr;157(4):272-5. doi: 10.1007/s004310050809. Eur J Pediatr. 1998. PMID: 9578959

7

Bone age in 116 untreated patients with Turner's syndrome rated by a computer-assisted method (CASAS).

Schwarze CP, Arens D, Haber HP, Wollmann HA, Binder G, Mayer EI, Ranke MB. Schwarze CP, et al. Among authors: binder g. Acta Paediatr. 1998 Nov;87(11):1146-50. doi: 10.1080/080352598750031130. Acta Paediatr. 1998. PMID: 9846916

8

Short-term increments of insulin-like growth factor I (IGF-I) and IGF-binding protein-3 predict the growth response to growth hormone (GH) therapy in GH-sensitive children.

Schwarze CP, Wollmann HA, Binder G, Ranke MB. Schwarze CP, et al. Among authors: binder g. Acta Paediatr Suppl. 1999 Feb;88(428):200-8. doi: 10.1111/j.1651-2227.1999.tb14392.x. Acta Paediatr Suppl. 1999. PMID: 10102080

9

Reduced human growth hormone (hGH) bioactivity without a defect of the GH-1 gene in three patients with rhGH responsive growth failure.

Binder G, Benz MR, Elmlinger M, Pflaum CD, Strasburger CJ, Ranke MB. Binder G, et al. Clin Endocrinol (Oxf). 1999 Jul;51(1):89-95. doi: 10.1046/j.1365-2265.1999.00744.x. Clin Endocrinol (Oxf). 1999. PMID: 10468970

10

Identification of short stature caused by SHOX defects and therapeutic effect of recombinant human growth hormone.

Binder G, Schwarze CP, Ranke MB. Binder G, et al. J Clin Endocrinol Metab. 2000 Jan;85(1):245-9. doi: 10.1210/jcem.85.1.6375. J Clin Endocrinol Metab. 2000. PMID: 10634394 Clinical Trial.

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