Paper

2000

55 : l'Allemand D, Tardy V, Gruters A, Schnabel D, Krude H, Morel Y.: How a Patient Homozygous for a 30-kb Deletion of the C4-CYP 21 Genomic Region Can Have a Nonclassic Form of 21-Hydroxylase Deficiency.
J Clin Endocrinol Metab. 2000 Dec;85(12):4562-4567.

54: Biebermann H, Schoneberg T, Krude H, Gudermann T, Gruters A.: Constitutively activating TSH-receptor mutations as a molecular cause of non-autoimmune hyperthyroidism in childhood.
Langenbecks Arch Surg. 2000 Oct;385(6):390-2.

53: Netchine I, Sobrier ML, Krude H, Schnabel D, Maghnie M, Marcos E, Duriez B, Cacheux V, Moers Av, Goossens M, Gruters A, Amselem S. Related Articles, Nucleotide: Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency.
Nat Genet. 2000 Jun;25(2):182-6.
PMID: 10835633; UI: 20296621

52: Kreissig R, Amthauer H, Krude H, Steinmueller P, Stroszczynski C, Hosten N, Grueters A, Felix R. Related Articles: The use of FDG-PET and CT for the staging of adrenocortical carcinoma in children.
Pediatr Radiol. 2000 May;30(5):306. No abstract available.
[MEDLINE record in process]
PMID: 10836591; UI: 20294580

51: Pasel K, Schulz A, Timmermann K, Linnemann K, Hoeltzenbein M, Jaaskelainen J, Gruters A, Filler G, Schoneberg T. Related Articles: Functional characterization of the molecular defects causing nephrogenic diabetes insipidus in eight families.
J Clin Endocrinol Metab. 2000 Apr;85(4):1703-10.
PMID: 10770218; UI: 20230987

1999

50: Krude H, Schnabel D, Luck W, Gruters A. Related Articles: Implications of the phenotype of POMC deficiency for the role of POMC-derived peptides in skin physiology.
Ann N Y Acad Sci. 1999 Oct 20;885:419-21. No abstract available.
PMID: 10816678; UI: 20276653

49: Biebermann H, Liesenkotter KP, Emeis M, Oblanden M, Gruters A. Related Articles: Severe congenital hypothyroidism due to a homozygous mutation of the betaTSH gene.
Pediatr Res. 1999 Aug;46(2):170-3.
PMID: 10447110; UI: 99374776

48: Gruters A, Krude H, Biebermann H, Liesenkotter KP, Schoneberg T, Gudermann T. Related Articles: Alterations of neonatal thyroid function.
Acta Paediatr Suppl. 1999 Feb;88(428):17-22. Review.
PMID: 10102047; UI: 99202275

47: Kohler B, Schumacher V, Schulte-Overberg U, Biewald W, Lennert T, l'Allemand D, Royer-Pokora B, Gruters A. Related Articles: Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene.
Pediatr Res. 1999 Feb;45(2):187-90.
PMID: 10022588; UI: 99145186

46: Gruters A. Related Articles: Ocular manifestations in children and adolescents with thyrotoxicosis.
Exp Clin Endocrinol Diabetes. 1999;107 Suppl 5:S172-4. Review.
PMID: 10614915; UI: 20080578

1998

45: Biebermann H, Schoneberg T, Schulz A, Krause G, Gruters A, Schultz G, Gudermann T. Related Articles: A conserved tyrosine residue (Y601) in transmembrane domain 5 of the human thyrotropin receptor serves as a molecular switch to determine G-protein coupling.
FASEB J. 1998 Nov;12(14):1461-71.
PMID: 9806755; UI: 99024075

44: Coyle B, Reardon W, Herbrick JA, Tsui LC, Gausden E, Lee J, Coffey R, Grueters A, Grossman4 A, Phelps PD, Luxon L, Kendall-Taylor P, Scherer SW, Trembath RC. Related Articles, Protein: Molecular analysis of the PDS gene in Pendred syndrome.
Hum Mol Genet. 1998 Jul;7(7):1105-12.
PMID: 9618167; UI: 98282236

43: Gruters A. Related Articles: [Screening and early detection of congenital hypothyroidism in Germany--still insufficient].
Internist (Berl). 1998 Jun;39(6):574-6. Review. German. No abstract available.
PMID: 9677511; UI: 98342475

42: Krude H, Biebermann H, Luck W, Horn R, Brabant G, Gruters A. Related Articles: Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans.
Nat Genet. 1998 Jun;19(2):155-7.
PMID: 9620771; UI: 98282093

41: Gruters A, Schoneberg T, Biebermann H, Krude H, Krohn HP, Dralle H, Gudermann T. Related Articles, Protein: Severe congenital hyperthyroidism caused by a germ-line neo mutation in the extracellular portion of the thyrotropin receptor.
J Clin Endocrinol Metab. 1998 May;83(5):1431-6.
PMID: 9589634; UI: 98251545

40: Macchia PE, Lapi P, Krude H, Pirro MT, Missero C, Chiovato L, Souabni A, Baserga M, Tassi V, Pinchera A, Fenzi G, Gruters A, Busslinger M, Di Lauro R. Related Articles, Protein, Nucleotide: PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis.
Nat Genet. 1998 May;19(1):83-6.
PMID: 9590296; UI: 98250178

39: Gruters A. Related Articles: Treatment of Graves' disease in children and adolescents.
Horm Res. 1998;49(6):255-7. Review. No abstract available.
PMID: 9623515; UI: 98284973

38: Schoneberg T, Schulz A, Biebermann H, Gruters A, Grimm T, Hubschmann K, Filler G, Gudermann T, Schultz G. Related Articles, Protein: V2 vasopressin receptor dysfunction in nephrogenic diabetes insipidus caused by different molecular mechanisms.
Hum Mutat. 1998;12(3):196-205.
PMID: 9711877; UI: 98375695

vor 1998

37: Biebermann H, Schoneberg T, Krude H, Schultz G, Gudermann T, Gruters A. Related Articles: Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism.
J Clin Endocrinol Metab. 1997 Oct;82(10):3471-80.
PMID: 9329388; UI: 97469971

36: Biebermann H, Gruters A, Schoneberg T, Gudermann T. Related Articles: Congenital hypothyroidism caused by mutations in the thyrotropin-receptor gene.
N Engl J Med. 1997 May 8;336(19):1390-1. No abstract available.
PMID: 9139226; UI: 97263452

35: Roth C, Siggelkow H, Gruters A, Hufner M, Lakomek M. Related Articles: [Neonatal Basedow's disease in twins from a mother with severe T3 hyperthyroidism].
Dtsch Med Wochenschr. 1997 May 2;122(18):572-7. German.
PMID: 9190309; UI: 97317526

34: Wilichowski E, Gruters A, Kruse K, Rating D, Beetz R, Korenke GC, Ernst BP, Christen HJ, Hanefeld F. Related Articles: Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndrome.
Pediatr Res. 1997 Feb;41(2):193-200. Review.
PMID: 9029638; UI: 97181477

33: Krude H, Biebermann H, Krohn HP, Dralle H, Gruters A. Related Articles: Congenital hyperthyroidism.
Exp Clin Endocrinol Diabetes. 1997;105 Suppl 4:6-11. Review.
PMID: 9439907; UI: 98103081

32: Gruters A, Liesenkotter KP, Zapico M, Jenner A, Dutting C, Pfeiffer E, Lehmkuhl U. Related Articles: Results of the screening program for congenital hypothyroidism in Berlin (1978-1995).
Exp Clin Endocrinol Diabetes. 1997;105 Suppl 4:28-31.
PMID: 9439911; UI: 98103085

31: Liesenkotter KP, Kiebler A, Stach B, Willgerodt H, Gruters A. Related Articles: Small thyroid volumes and normal iodine excretion in Berlin schoolchildren indicate full normalization of iodine supply.
Exp Clin Endocrinol Diabetes. 1997;105 Suppl 4:46-50.
PMID: 9439915; UI: 98103089

30: Stoeva I, Peneva L, Grigorova R, Vassileva B, Brumm H, Gruters A. Related Articles: Neonatal TSH screening--an instrument of iodine supplementation monitoring in Bulgaria in comparison to Berlin--a preliminary report.
Exp Clin Endocrinol Diabetes. 1997;105 Suppl 4:51-4.
PMID: 9439916; UI: 98103090

29: l'Allemand D, Keller E, Hoeppner W, Serban A, Morel Y, Gruters A. Related Articles: Nonclassical adrenal hyperplasia due to 21-hydroxylase-deficiency: does genotyping predict the clinical manifestation?
Endocr Res. 1996 Nov;22(4):735-9.
PMID: 8969935; UI: 97124799

28: Herrmann ME, Dannemann A, Gruters A, Radisch B, Dudenhausen JW, Bergmann R, Coumbos A, Weitzel HK, Wahn U. Related Articles: Prospective study of the atopy preventive effect of maternal avoidance of milk and eggs during pregnancy and lactation.
Eur J Pediatr. 1996 Sep;155(9):770-4.
PMID: 8874109; UI: 97028022

27: Liesenkotter KP, Gopel W, Bogner U, Stach B, Gruters A. Related Articles: Earliest prevention of endemic goiter by iodine supplementation during pregnancy.
Eur J Endocrinol. 1996 Apr;134(4):443-8.
PMID: 8640295; UI: 96224955

26: Kohler B, Schnabel D, Biebermann H, Gruters A. Related Articles: Transient congenital hypothyroidism and hyperthyrotropinemia: normal thyroid function and physical development at the ages of 6-14 years.
J Clin Endocrinol Metab. 1996 Apr;81(4):1563-7.
PMID: 8636368; UI: 96186166

25: Gopel W, Schnabel D, Volger S, Gruters A. Related Articles: Severe hypokalaemia due to hyperreninaemia and secondary hyperaldosteronism in a boy with pheochromocytoma.
Eur J Pediatr. 1996 Feb;155(2):147-8. No abstract available.
PMID: 8775235; UI: 96371400

24: Krude H, Biebermann H, Gopel W, Gruters A. Related Articles: The gene for the thyrotropin receptor (TSHR) as a candidate gene for congenital hypothyroidism with thyroid dysgenesis.
Exp Clin Endocrinol Diabetes. 1996;104 Suppl 4:117-20. Review.
PMID: 8981017; UI: 97135480

23: Gruters A, Kohler B, Wolf A, Soling A, de Vijlder L, Krude H, Biebermann H. Related Articles: Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism.
Exp Clin Endocrinol Diabetes. 1996;104 Suppl 4:121-3.
PMID: 8981018; UI: 97135481

22: Schwab KO, Sohlemann P, Gerlich M, Broecker M, Petrykowski W, Holzapfel HP, Paschke R, Gruters A, Derwahl M. Related Articles: Mutations of the TSH receptor as cause of congenital hyperthyroidism.
Exp Clin Endocrinol Diabetes. 1996;104 Suppl 4:124-8.
PMID: 8981019; UI: 97135482

21: Gruters A, Liesenkotter KP, Willgerodt H. Related Articles: Persistence of differences in iodine status in newborns after the reunification of Berlin.
N Engl J Med. 1995 Nov 23;333(21):1429. No abstract available.
PMID: 7477142; UI: 96043665

20: Sperling K, Pelz J, Wegner RD, Dorries A, Gruters A, Mikkelsen M. Related Articles: Fallout from Chernobyl. Authors stand by study that Chernobyl increased trisomy 21 in Berlin.
BMJ. 1994 Nov 12;309(6964):1299. No abstract available.
PMID: 7741909; UI: 95195452

19: Sperling K, Pelz J, Wegner RD, Dorries A, Gruters A, Mikkelsen M. Related Articles: Significant increase in trisomy 21 in Berlin nine months after the Chernobyl reactor accident: temporal correlation or causal relation?
BMJ. 1994 Jul 16;309(6948):158-62.
PMID: 8044094; UI: 94319239

18: Gruters A, Delange F, Giovannelli G, Klett M, Rochiccioli P, Torresani T, Grant D, Hnikova O, Maenpaa J, Rondanini GF, et al. Related Articles: Guidelines for neonatal screening programs for congenital hypothyroidism. European Society for Pediatric Endocrinology Working Group on Congenital Hypothyroidism.
Horm Res. 1994;41(1):1-2. No abstract available.
PMID: 8013935; UI: 94283930

17: Gruters A, Finke R, Krude H, Meinhold H. Related Articles: Etiological grouping of permanent congenital hypothyroidism with a thyroid gland in situ.
Horm Res. 1994;41(1):3-9. Review. No abstract available.
PMID: 8013940; UI: 94283935

16: Gruters A, Delange F, Giovannelli G, Klett M, Rochiccioli P, Torresani T, Grant D, Hnikova O, Maenpaa J, Rondanini GF, et al. Related Articles: Guidelines for neonatal screening programmes for congenital hypothyroidism. Working group on congenital hypothyroidism of the European Society for Paediatric Endocrinology.
Eur J Pediatr. 1993 Dec;152(12):974-5. No abstract available.
PMID: 8131813; UI: 94178329

15: Monch E, Gruters A. Related Articles: [Screening of newborns].
Dtsch Krankenpflegez. 1993 Feb;46(2):77-9. German. No abstract available.
PMID: 8449158; UI: 93193620

14: Gruters A. Related Articles: Congenital hypothyroidism.
Pediatr Ann. 1992 Jan;21(1):15, 18-21, 24-8. Review.
PMID: 1549396; UI: 92195726

13: Schleusener H, Bogner U, Peters H, Kotulla P, Schmieg D, Gruters A, Mayr WR. Related Articles: The relevance of genetic susceptibility in Graves' disease and immune thyroiditis.
Exp Clin Endocrinol. 1991 May;97(2-3):127-32. Review.
PMID: 1915624; UI: 92008306

12: Toublanc JE, Gruters A, Bogner U, Fulla Y, Dugue MA. Related Articles: [Study of antibody-dependent cell mediated cytotoxicity and thyroid growth blocking antibodies in congenital hypothyroidism].
Arch Fr Pediatr. 1991 Feb;48(2):89-94. French.
PMID: 2048951; UI: 91264567

11: Gruters A, Heidemann P, Schluter H, Stubbe P, Weber B, Helge H. Related Articles: Effect of different oestrogen doses on final height reduction in girls with constitutional tall stature.
Eur J Pediatr. 1989 Oct;149(1):11-3.
PMID: 2606121; UI: 90108024

10: Bogner U, Gruters A, Sigle B, Helge H, Schleusener H. Related Articles: Cytotoxic antibodies in congenital hypothyroidism.
J Clin Endocrinol Metab. 1989 Mar;68(3):671-5.
PMID: 2645314; UI: 89139790

9: Danne T, Gruters A, Schuppan D, Quantas N, Enders I, Weber B. Related Articles: Relationship of procollagen type III propeptide-related antigens in serum to somatic growth in healthy children and patients with growth disorders.
J Pediatr. 1989 Feb;114(2):257-60. No abstract available.
PMID: 2915284; UI: 89125211

8: Rother K, Zachmann M, Kempken B, Gruters A, Schnabel D, L'Allemand D, Hausler G, Frisch H. Related Articles: Effect of recombinant human growth hormone on urinary 15N-nitrogen balance in girls with Turner syndrome as compared to children with growth hormone deficiency.
Horm Res. 1989;32(5-6):166-9.
PMID: 2634609; UI: 90236415

7: Danne T, Gruters A, Schnabel K, Burger W, L'Allemand D, Enders I, Helge H, Weber B. Related Articles: Long-term monitoring of treatment with recombinant human growth hormone by serial determinations of type III procollagen-related antigens in serum.
Pediatr Res. 1988 Feb;23(2):167-71.
PMID: 3353159; UI: 88176222

6: l'Allemand D, Gruters A, Beyer P, Weber B. Related Articles: Iodine in contrast agents and skin disinfectants is the major cause for hypothyroidism in premature infants during intensive care.
Horm Res. 1987;28(1):42-9.
PMID: 3447940; UI: 88197058

5: Grueters A, Lakshmanan J, Tarris R, Alm J, Fisher DA. Related Articles: Nerve growth factor in mouse milk during early lactation: lack of dependency on submandibular salivary glands.
Pediatr Res. 1985 Sep;19(9):934-7.
PMID: 4047763; UI: 86015799

4: Grueters A, Alm J, Lakshmanan J, Fisher DA. Related Articles: Epidermal growth factor in mouse milk during early lactation: lack of dependency on submandibular glands.
Pediatr Res. 1985 Aug;19(8):853-6.
PMID: 3875831; UI: 85297546

3: Lakshmanan J, Perheentupa J, Hoath SB, Kim H, Gruters A, Odell C, Fisher DA. Related Articles: Epidermal growth factor in mouse ocular tissue: effects of thyroxine and exogenous epidermal growth factor.
Pediatr Res. 1985 Mar;19(3):315-9.
PMID: 3872442; UI: 85165126

2: Lakshmanan J, Beri U, Perheentupa J, Grueters A, Kim H, Macaso T, Fisher DA. Related Articles: Acquisition of submandibular gland nerve growth factor (SMG-NGF) responsiveness to thyroxine administration in neonatal mice.
J Neurosci Res. 1984;12(1):71-85.
PMID: 6207304; UI: 85009768

1: Gruters A, l'Allemand D, Heidemann PH, Schurnbrand P. Related Articles: Incidence of iodine contamination in neonatal transient hyperthyrotropinemia.
Eur J Pediatr. 1983 Sep;140(4):299-300.
PMID: 6628451; UI: 84028752