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Items: 1 to 50 of 86

1.

First Observation of Cross-Beam Energy Transfer Mitigation for Direct-Drive Inertial Confinement Fusion Implosions Using Wavelength Detuning at the National Ignition Facility.

Marozas JA, Hohenberger M, Rosenberg MJ, Turnbull D, Collins TJB, Radha PB, McKenty PW, Zuegel JD, Marshall FJ, Regan SP, Sangster TC, Seka W, Campbell EM, Goncharov VN, Bowers MW, Di Nicola JG, Erbert G, MacGowan BJ, Pelz LJ, Yang ST.

Phys Rev Lett. 2018 Feb 23;120(8):085001. doi: 10.1103/PhysRevLett.120.085001.

PMID:
29543010
2.

The IgCAM CLMP regulates expression of Connexin43 and Connexin45 in intestinal and ureteral smooth muscle contraction 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 Feb 22;11(2). pii: dmm032128. doi: 10.1242/dmm.032128.

3.

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
4.

Robustness of spatial-coherence multiplexing under receiver misalignment.

Pelz LJ, Anderson BL.

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

PMID:
18268657
5.

Sexual maturation in East German boys.

Willers B, Engelhardt L, Pelz L.

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

PMID:
8819542
6.
7.

Sexual maturation in East German girls.

Engelhardt L, Willers B, Pelz L.

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

PMID:
8645951
8.

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
9.

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
10.

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
11.

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
12.
13.

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
14.

Menarcheal age in East German girls.

Pelz L.

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

PMID:
1467624
15.

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
16.

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
17.

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
18.

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
19.

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
20.

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

Pelz L, Stein B.

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

PMID:
2376938
21.

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

Pelz L, Stein B.

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

PMID:
2377374
22.

[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
23.

[Familial Noonan syndrome].

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

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

PMID:
2747123
24.

[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
25.

[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
26.

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
27.

[The intermamillary index of newborn infants].

Pelz L, Richter C.

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

PMID:
2724783
28.

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
29.

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
30.

Isochromosome (18q) in siblings.

Krüger G, Götz J, Dunker H, Pelz L.

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

PMID:
3677464
31.

The Greig cephalopolysyndactyly syndrome.

Pelz L, Krüger G, Götz J.

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

PMID:
3025136
32.
33.

[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
34.

[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
35.

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
36.

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
37.

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
39.

[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
40.

[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
41.

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
42.

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
43.

[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
44.

[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
45.

[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
46.
47.

[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
48.

[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
49.

[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
50.

[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

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