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Items: 1 to 50 of 85

1.

The IgCAM CLMP is required for intestinal and ureteral smooth muscle contraction by regulating Connexin43 and 45 expression in mice.

Langhorst H, Jüttner R, Groneberg D, Mohtashamdolatshahi A, Pelz L, Purfürst B, Schmidt-Ott KM, Friebe A, Rathjen FG.

Dis Model Mech. 2018 Jan 19. pii: dmm.032128. doi: 10.1242/dmm.032128. [Epub ahead of print]

2.

The cell adhesion molecule BT-IgSF is essential for a functional blood-testis barrier and male fertility in mice.

Pelz L, Purfürst B, Rathjen FG.

J Biol Chem. 2017 Dec 29;292(52):21490-21503. doi: 10.1074/jbc.RA117.000113. Epub 2017 Nov 9.

PMID:
29123028
3.

Robustness of spatial-coherence multiplexing under receiver misalignment.

Pelz LJ, Anderson BL.

Appl Opt. 1998 Feb 10;37(5):815-20.

PMID:
18268657
4.

Sexual maturation in East German boys.

Willers B, Engelhardt L, Pelz L.

Acta Paediatr. 1996 Jul;85(7):785-8.

PMID:
8819542
5.
6.

Sexual maturation in East German girls.

Engelhardt L, Willers B, Pelz L.

Acta Paediatr. 1995 Dec;84(12):1362-5.

PMID:
8645951
7.

Spatial-coherence modulation for optical interconnections.

Anderson BL, Pelz LJ.

Appl Opt. 1995 Nov 10;34(32):7443-50. doi: 10.1364/AO.34.007443.

PMID:
21060617
8.

Auriculocephalic index: a new anthropometric index for syndrome delineation.

Pelz L, Stein B.

Am J Med Genet. 1995 Jan 30;55(3):257-60.

PMID:
7726218
9.

Esophageal stenosis in acrocephalosyndactyly type I.

Pelz L, Unger K, Radke M.

Am J Med Genet. 1994 Oct 15;53(1):91. No abstract available.

PMID:
7802047
10.

Cytomegalic type of congenital adrenal hypoplasia due to autosomal recessive inheritance.

Krüger G, Mix M, Pelz L, Dunker H.

Am J Med Genet. 1993 Jun 1;46(4):475. No abstract available.

PMID:
8357028
11.
12.

Transmission of Proteus syndrome from mother to son?

Krüger G, Pelz L, Wiedemann HR.

Am J Med Genet. 1993 Jan 1;45(1):117-8. No abstract available.

PMID:
8418646
13.

Menarcheal age in East German girls.

Pelz L.

Acta Paediatr. 1992 Nov;81(11):946-7. No abstract available.

PMID:
1467624
14.

A somatic cell hybrid panel and DNA probes for physical mapping of human chromosome 7p.

Vortkamp A, Thias U, Gessler M, Rosenkranz W, Kroisel PM, Tommerup N, Krüger G, Götz J, Pelz L, Grzeschik KH.

Genomics. 1991 Nov;11(3):737-43.

PMID:
1663489
15.

Mitral valve and tricuspidal valve prolapse in Melnick-Needles syndrome.

Krüger G, Schumacher K, Erfurt F, Pelz L.

Eur J Pediatr. 1991 Oct;150(12):858. No abstract available.

PMID:
1743220
16.

Delayed spontaneous pubertal growth spurt in girls with the Ullrich-Turner syndrome.

Pelz L, Sager G, Hinkel GK, Kirchner M, Krüger G, Verron G.

Am J Med Genet. 1991 Sep 15;40(4):401-5.

PMID:
1746600
17.

Long-term follow-up in females with Ullrich-Turner syndrome.

Pelz L, Köbschall H, Lübcke UG, Krüger G, Hinkel GK, Verron G.

Clin Genet. 1991 Jul;40(1):1-5.

PMID:
1884512
18.

VACTERL-association: an unusual case of fetus detected by ultrasound screening at 19 weeks of gestation.

Krüger G, Külz T, Dunker H, Pelz L.

Eur J Pediatr. 1990 Aug;149(11):809. No abstract available.

PMID:
2226560
19.

[Clinical evaluation of testicular size in boys and adolescents].

Pelz L, Stein B.

Kinderarztl Prax. 1990 May;58(5):241-6. German.

PMID:
2376938
20.

[Clinical assessment of ear size in children and adolescents].

Pelz L, Stein B.

Padiatr Grenzgeb. 1990;29(3):229-35. German.

PMID:
2377374
21.

[A staged plan for laboratory diagnosis of hereditary metabolic diseases].

Zöllner H, Tittelbach-Helmrich W, Bannert N, Cario WR, Pelz L, Seidlitz G, Cobet G, Wiedemann G, Zinsmeyer J, Beier L, et al.

Kinderarztl Prax. 1989 Dec;57(12):623-6. German.

PMID:
2625844
22.

[Familial Noonan syndrome].

Krüger G, Schumacher K, Mix M, Pelz L.

Kinderarztl Prax. 1989 May;57(5):245-8. German.

PMID:
2747123
23.

[Cytogenetic detection of Prader-Willi syndrome in infancy].

Götz J, Krüger G, Westphal BC, Pelz L.

Kinderarztl Prax. 1989 May;57(5):239-43. German.

PMID:
2747122
24.

[Ullrich-Turner syndrome and anorexia nervosa--an association?].

Mix VM, Krüger G, Richter I, Pelz L, Cammon R.

Kinderarztl Prax. 1989 May;57(5):235-8. German.

PMID:
2747121
25.

Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13).

Krüger G, Götz J, Kvist U, Dunker H, Erfurth F, Pelz L, Zech L.

Am J Med Genet. 1989 Mar;32(3):411-6.

PMID:
2729360
26.

[The intermamillary index of newborn infants].

Pelz L, Richter C.

Kinderarztl Prax. 1989 Mar;57(3):129-32. German.

PMID:
2724783
27.

Increased methotrexate-induced chromosome breakage in patients with free trisomy 21 and their parents.

Pelz L, Götz J, Krüger G, Witt G.

Hum Genet. 1988 Dec;81(1):38-40.

PMID:
2974013
28.

New aspects of oestrogen/gestagen-induced growth and endocrine changes in individuals with Turner syndrome.

Pelz L.

Eur J Pediatr. 1988 Aug;147(6):663-4. No abstract available.

PMID:
3181211
29.

Isochromosome (18q) in siblings.

Krüger G, Götz J, Dunker H, Pelz L.

Clin Genet. 1987 Oct;32(4):249-53.

PMID:
3677464
30.

The Greig cephalopolysyndactyly syndrome.

Pelz L, Krüger G, Götz J.

Helv Paediatr Acta. 1986 Oct;41(4):381-2. No abstract available.

PMID:
3025136
31.
32.

[Effect of mestranol and chlormadinone acetate on basal and TRH-stimulated PRL secretion in Turner's syndrome].

Rudolf K, Kunkel S, Pelz L.

Zentralbl Gynakol. 1985;107(23):1446-53. German.

PMID:
2420101
33.

[Proposed international nomenclature for dysmorphogenesis].

Rupprecht E, Pelz L, Nitz I.

Radiol Diagn (Berl). 1984;25(6):785-7. German. No abstract available.

PMID:
6522588
34.

Neonatal intensive care does not cause chromosome damage.

Méhes K, Pelz L, Kosztolányi G, Bajnóczky K, Meggyessy V, Uhlemann M.

Acta Paediatr Hung. 1984;25(3):271-4.

PMID:
6498008
35.

A new type of familial chromosome translocation involving 3p and 6q in two unrelated families.

Gottschall A, Losan F, Pelz L, Wiedersberg H.

Hum Genet. 1983;64(3):304. No abstract available.

PMID:
6885078
36.

Body height in Turner's syndrome.

Pelz L, Timm D, Eyermann E, Hinkel GK, Kirchner M, Verron G.

Clin Genet. 1982 Aug;22(2):62-6.

PMID:
7172479
38.

[Retinopathy of the premature: possibility and limitations of prevention, therapy and metaphylaxis].

Uhlemann M, Plath C, Eichler J, Pelz L, Pohl H.

Z Arztl Fortbild (Jena). 1982 Jun 15;76(12):558-60. German. No abstract available.

PMID:
7124025
39.

[Body height in Ullrich-Turner syndrome. Pathognomonic growth functions].

Pelz L, Sussmann S, Timm D.

Kinderarztl Prax. 1981 Apr;49(4):206-12. German. No abstract available.

PMID:
7253409
40.

Responsiveness of the pituitary to stimulation with arginine, GRH and TRH in patients with Turner' syndrome (karyotype 45, XO).

Kunkel S, Rudolf K, Kyank H, Woltanski P, Pelz L.

Acta Univ Palacki Olomuc Fac Med. 1981;101:84-9. No abstract available.

PMID:
6211058
41.

Responsiveness of the pituitary to stimulation with arginine, GRH and TRH in patients with Turner's syndrome (karyotype 45, XO).

Kunkel S, Rudolf K, Kyank H, Woltanski P, Pelz L.

Acta Univ Palacki Olomuc Fac Med. 1981;101:84-9. No abstract available.

PMID:
6085921
42.

[Results and consequences of a social medical study in the region of Gera on Langdon-Down disease].

Kirchner M, Wolfram E, Pröhl U, Pelz L, Mücke J, Sandig KR, Seidlitz G.

Kinderarztl Prax. 1980 Nov;48(11):571-82. German. No abstract available.

PMID:
6450294
43.

[Indications and contra-indications for cytogenetic studies in childhood and adolescence].

Pelz L, Mücke J, Federlein F, Gedschoid J, Kirchner M, Mieler W, Sandig KR, Steinbicker V.

Kinderarztl Prax. 1980 Oct;48(10):548-50. German. No abstract available.

PMID:
7441994
44.

[Diagnostic value of the intermamillary index for the early diagnosis of the Shereshevskiĭ-Turner syndrome].

Pelz L, Tornov B.

Pediatriia. 1980 Feb;(2):40-1. Russian. No abstract available.

PMID:
7360589
45.
46.

[Experience obtained from intra-uterine foetal transfusion to cope with severe rhesus-caused haemolytic disease of foetus - ten-year report (author's transl)].

Klausch B, Kyank H, Hille M, Müller S, Stark KH, Plesse R, Pelz L.

Zentralbl Gynakol. 1980;102(13):689-701. German.

PMID:
7445825
47.

[Possibilities of an early diagnosis of hereditary diseases].

Pelz L.

Z Arztl Fortbild (Jena). 1978 Jun 15;72(11-12):539-41. German. No abstract available.

PMID:
676363
48.

[Intersexual organ abnormalities in childhood. III. Sex assignment and principles of medical treatment].

Pelz L, Sandig KR, Hoepffner W, Kirchner M, Kotte W, Lässig W, Metzke H, Schmalz H, Schüttauf J, Seidlitz G, Steinbicker V, Stolpe HJ, Warbanow B.

Kinderarztl Prax. 1978 May;46(5):258-65. German. No abstract available.

PMID:
672030
49.

[Intersexual organ malformations in childhood. II. Frequency and clinical aspects, including differential diagnosis].

Sandig KR, Pelz L, Hoepffner W, Kirchner M, Kotte W, Lässig W, Metzke H, Schmalz H, Schüttauf J, Seidlitz G, Steinbicker V, Stolpe HJ, Warbanow B.

Kinderarztl Prax. 1978 Jan;46(1):27-36. German. No abstract available.

PMID:
651135
50.

[Intersexual organ malformations in childhood. I. Definition, classification, problems and diagnosis].

Sandig KR, Pelz L, Hoepffner W, Kirchner M, Kotte W, Lässig W, Metzke H, Schmalz H, Schüttauf J, Seidlitz G, Steinbicker V, Stolpe HJ, Warbanow B.

Kinderarztl Prax. 1977 Dec;45(12):529-34. German. No abstract available.

PMID:
609195

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