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Items: 1 to 50 of 59

1.

Quantification of PpIX-fluorescence of cerebral metastases: a pilot study.

Knipps J, Fischer I, Neumann LM, Rapp M, Dibué-Adjei M, Freiin von Saß C, Placke JM, Mijderwijk HJ, Steiger HJ, Sabel M, Cornelius JF, Kamp MA.

Clin Exp Metastasis. 2019 Oct;36(5):467-475. doi: 10.1007/s10585-019-09986-x. Epub 2019 Aug 2.

PMID:
31376098
2.

Is the Intensity of 5-Aminolevulinic Acid-Derived Fluorescence Related to the Light Source?

Kamp MA, Knipps J, Neumann LM, Mijderwijk HJ, Dibué-Adjei M, Steiger HJ, Slotty PJ, Rapp M, Cornelius JF, Sabel M.

World Neurosurg. 2019 Nov;131:e271-e276. doi: 10.1016/j.wneu.2019.07.136. Epub 2019 Jul 24.

PMID:
31351208
3.

Gut microbiome differences between wild and captive black rhinoceros - implications for rhino health.

Gibson KM, Nguyen BN, Neumann LM, Miller M, Buss P, Daniels S, Ahn MJ, Crandall KA, Pukazhenthi B.

Sci Rep. 2019 May 28;9(1):7570. doi: 10.1038/s41598-019-43875-3.

4.

Quantification of ALA-fluorescence induced by a modified commercially available head lamp and a surgical microscope.

Sabel M, Knipps J, Neumann LM, Kieslich M, Steiger HJ, Rapp M, Kamp MA.

Neurosurg Rev. 2018 Oct;41(4):1079-1083. doi: 10.1007/s10143-018-0997-2. Epub 2018 Jul 23. No abstract available.

PMID:
30039396
5.

Fluorescence Behavior and Dural Infiltration of Meningioma Analyzed by 5-Aminolevulinic Acid-Based Fluorescence: Operating Microscope Versus Mini-Spectrometer.

Knipps J, Beseoglu K, Kamp M, Fischer I, Felsberg J, Neumann LM, Steiger HJ, Cornelius JF.

World Neurosurg. 2017 Dec;108:118-127. doi: 10.1016/j.wneu.2017.08.140. Epub 2017 Sep 1.

PMID:
28866060
6.

Efficacy of 5-aminolevulinic acid based photodynamic therapy in pituitary adenomas-experimental study on rat and human cell cultures.

Neumann LM, Beseoglu K, Slotty PJ, Senger B, Kamp MA, Hänggi D, Steiger HJ, Cornelius JF.

Photodiagnosis Photodyn Ther. 2016 Jun;14:77-83. doi: 10.1016/j.pdpdt.2016.02.006. Epub 2016 Feb 22.

PMID:
26906188
7.

Lymphatic fluid for the detection of Mycobacterium avium subsp. paratuberculosis in cows by PCR, compared to fecal sampling and detection of antibodies in blood and milk.

Khol JL, Pinedo PJ, Buergelt CD, Neumann LM, Rae DO.

Vet Microbiol. 2014 Aug 6;172(1-2):301-8. doi: 10.1016/j.vetmic.2014.05.022. Epub 2014 May 29.

PMID:
24930984
8.

NBDE Part II practice analyses: an overview.

Tsai TH, Kramer GA, Yang CL, Neumann LM, Chang SR.

J Dent Educ. 2013 Dec;77(12):1566-80.

9.

Validating the standard for the National Board Dental Examination Part II.

Tsai TH, Neumann LM, Littlefield JH.

J Dent Educ. 2012 May;76(5):540-4.

10.

Assessing context effects on test validity of the National Board Dental Examination Part I.

Yang CL, Neumann LM, Kramer GA.

J Dent Educ. 2012 Apr;76(4):395-406.

11.

The collection of lymphatic fluid from the bovine udder and its use for the detection of Mycobacterium avium subsp. paratuberculosis in the cow.

Khol JL, Pinedo PJ, Buergelt CD, Neumann LM, Baumgartner W, Rae DO.

J Vet Diagn Invest. 2012 Jan;24(1):23-31. doi: 10.1177/1040638711425943. Epub 2011 Dec 6.

PMID:
22362932
12.

Generalizability analyses of NBDE Part II.

Tsai TH, Shin CD, Neumann LM, Grau BW.

Eval Health Prof. 2012 Jun;35(2):169-81. doi: 10.1177/0163278711425382. Epub 2011 Dec 7.

PMID:
22158689
13.

An investigation of the relationship between fecal and rumen bacterial concentrations in sheep.

Neumann LM, Dehority BA.

Zoo Biol. 2008 Mar;27(2):100-8. doi: 10.1002/zoo.20166.

PMID:
19360608
14.

Dental student assessment toolbox.

Kramer GA, Albino JE, Andrieu SC, Hendricson WD, Henson L, Horn BD, Neumann LM, Young SK.

J Dent Educ. 2009 Jan;73(1):12-35. No abstract available.

15.

Assessing dental students' competence: best practice recommendations in the performance assessment literature and investigation of current practices in predoctoral dental education.

Albino JE, Young SK, Neumann LM, Kramer GA, Andrieu SC, Henson L, Horn B, Hendricson WD.

J Dent Educ. 2008 Dec;72(12):1405-35. Review.

16.

Does faculty development enhance teaching effectiveness?

Hendricson WD, Anderson E, Andrieu SC, Chadwick DG, Cole JR, George MC, Glickman GN, Glover JF, Goldberg JS, Haden NK, Kalkwarf KL, Meyerowitz C, Neumann LM, Pyle M, Tedesco LA, Valachovic RW, Weaver RG, Winder RL, Young SK.

J Dent Educ. 2007 Dec;71(12):1513-33.

17.
18.

Revisiting the National Board Dental Examination.

Neumann LM, Macneil RL.

J Dent Educ. 2007 Oct;71(10):1281-92.

19.

Hay-Wells syndrome in a child with mutation in the TP73L gene.

Garcia Bartels N, Neumann LM, Mleczko A, Rubach K, Peters H, Rossi R, Sterry W, Blume-Peytavi U.

J Dtsch Dermatol Ges. 2007 Oct;5(10):919-23. English, German.

PMID:
17910675
20.

Validation of the National Board Dental Hygiene Examination.

Kramer GA, Neumann LM.

J Dent Hyg. 2007 Summer;81(3):63. Epub 2007 Jul 1.

PMID:
17908419
21.

Neuroendocrine tumor of the pancreas and bilateral adrenal pheochromocytomas. A rare manifestation of von Hippel-Lindau disease in childhood.

Langrehr JM, Bahra M, Kristiansen G, Neumann HP, Neumann LM, Plöckinger U, Lopez-Hänninen E.

J Pediatr Surg. 2007 Jul;42(7):1291-4.

PMID:
17618900
22.

Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome.

Klopocki E, Schulze H, Strauss G, Ott CE, Hall J, Trotier F, Fleischhauer S, Greenhalgh L, Newbury-Ecob RA, Neumann LM, Habenicht R, König R, Seemanova E, Megarbane A, Ropers HH, Ullmann R, Horn D, Mundlos S.

Am J Hum Genet. 2007 Feb;80(2):232-40. Epub 2006 Dec 21.

23.

Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation.

Kalscheuer VM, FitzPatrick D, Tommerup N, Bugge M, Niebuhr E, Neumann LM, Tzschach A, Shoichet SA, Menzel C, Erdogan F, Arkesteijn G, Ropers HH, Ullmann R.

Hum Genet. 2007 May;121(3-4):501-9. Epub 2007 Jan 9.

PMID:
17211639
24.

Interest and responsibility of ADA in dental licensure.

Jones TH, Neumann LM, Haglund LJ.

J Evid Based Dent Pract. 2006 Mar;6(1):143-7.

PMID:
17138418
25.

Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13.

Tonnies H, Gerlach A, Heineking B, Starke H, Neitzel H, Neumann LM.

Cytogenet Genome Res. 2006;114(3-4):325-9.

PMID:
16954674
26.

A complex phenotype with cystic renal disease.

Müller D, Klopocki E, Neumann LM, Mundlos S, Taupitz M, Schulze I, Ropers HH, Querfeld U, Ullmann R.

Kidney Int. 2006 Nov;70(9):1656-60. Epub 2006 Aug 16. No abstract available.

27.

Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene.

Klopocki E, Neumann LM, Tönnies H, Ropers HH, Mundlos S, Ullmann R.

Eur J Hum Genet. 2006 Dec;14(12):1274-9. Epub 2006 Aug 9.

28.

[Ocular manifestations and surgical results in patients with Marfan syndrome].

Ladewig MS, Robinson PN, Neumann LM, Holz FG, Foerster MH.

Ophthalmologe. 2006 Sep;103(9):777-82. German.

PMID:
16819661
29.

Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein-Taybi syndrome.

Bartsch O, Rasi S, Delicado A, Dyack S, Neumann LM, Seemanová E, Volleth M, Haaf T, Kalscheuer VM.

Hum Genet. 2006 Sep;120(2):179-86. Epub 2006 Jun 17.

PMID:
16783566
30.

Dyggve-Melchior-Clausen syndrome and Smith-McCort dysplasia: clinical and molecular findings in three families supporting genetic heterogeneity in Smith-McCort dysplasia.

Neumann LM, El Ghouzzi V, Paupe V, Weber HP, Fastnacht E, Leenen A, Lyding S, Klusmann A, Mayatepek E, Pelz J, Cormier-Daire V.

Am J Med Genet A. 2006 Mar 1;140(5):421-6.

PMID:
16470731
31.

Smith-Lemli-Opitz syndrome with a classical phenotype, oesophageal achalasia and borderline plasma sterol concentrations.

Haas D, Armbrust S, Haas JP, Zschocke J, Mühlmann K, Fusch C, Neumann LM.

J Inherit Metab Dis. 2005;28(6):1191-6.

PMID:
16435228
32.

An Ehlers-Danlos syndrome type VIA patient with cystic malformations of the meninges.

Yeowell HN, Walker LC, Neumann LM.

Eur J Dermatol. 2005 Sep-Oct;15(5):353-8.

PMID:
16172044
33.

Restrictive dermopathy associated with transposition of the great arteries and microcolon: a rare neonatal entity with new symptoms.

Armbrust S, Hoffmann R, Jochum F, Neumann LM, Fusch C.

Arch Dermatol. 2005 May;141(5):611-3.

PMID:
15897383
34.

Shprintzen-Goldberg syndrome: fourteen new patients and a clinical analysis.

Robinson PN, Neumann LM, Demuth S, Enders H, Jung U, König R, Mitulla B, Müller D, Muschke P, Pfeiffer L, Prager B, Somer M, Tinschert S.

Am J Med Genet A. 2005 Jun 15;135(3):251-62.

PMID:
15884042
35.

Trends in dental and allied dental education.

Neumann LM.

J Am Dent Assoc. 2004 Sep;135(9):1253-9.

PMID:
15493389
36.

Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: an autosomal recessive syndrome.

Zenker M, Tralau T, Lennert T, Pitz S, Mark K, Madlon H, Dötsch J, Reis A, Müntefering H, Neumann LM.

Am J Med Genet A. 2004 Oct 1;130A(2):138-45. Review.

PMID:
15372515
37.

Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities.

Zenker M, Aigner T, Wendler O, Tralau T, Müntefering H, Fenski R, Pitz S, Schumacher V, Royer-Pokora B, Wühl E, Cochat P, Bouvier R, Kraus C, Mark K, Madlon H, Dötsch J, Rascher W, Maruniak-Chudek I, Lennert T, Neumann LM, Reis A.

Hum Mol Genet. 2004 Nov 1;13(21):2625-32. Epub 2004 Sep 14.

PMID:
15367484
38.

Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation.

Teber OA, Gillessen-Kaesbach G, Fischer S, Böhringer S, Albrecht B, Albert A, Arslan-Kirchner M, Haan E, Hagedorn-Greiwe M, Hammans C, Henn W, Hinkel GK, König R, Kunstmann E, Kunze J, Neumann LM, Prott EC, Rauch A, Rott HD, Seidel H, Spranger S, Sprengel M, Zoll B, Lohmann DR, Wieczorek D.

Eur J Hum Genet. 2004 Nov;12(11):879-90.

39.

Mutations in microcephalin cause aberrant regulation of chromosome condensation.

Trimborn M, Bell SM, Felix C, Rashid Y, Jafri H, Griffiths PD, Neumann LM, Krebs A, Reis A, Sperling K, Neitzel H, Jackson AP.

Am J Hum Genet. 2004 Aug;75(2):261-6. Epub 2004 Jun 15.

40.

Unexpected death of a 12 year old boy with monosomy 1p36.

Neumann LM, Polster T, Spantzel T, Bartsch O.

Genet Couns. 2004;15(1):19-26.

PMID:
15083695
41.

Ehlers-Danlos syndrome type VI with cystic malformations of the meninges in a 7-year-old girl.

Brunk I, Stöver B, Ikonomidou C, Brinckmann J, Neumann LM.

Eur J Pediatr. 2004 Apr;163(4-5):214-7. Epub 2004 Feb 11.

PMID:
14872341
42.

Spontaneous intracerebral hemorrhage and multiple infarction in Williams-Beuren syndrome.

Kalbhenn T, Neumann LM, Lanksch WR, Haberl H.

Pediatr Neurosurg. 2003 Dec;39(6):335-8.

PMID:
14734869
43.
45.

Prenatal diagnosis of Alagille syndrome.

Witt H, Neumann LM, Grollmuss O, Luck W, Becker M.

J Pediatr Gastroenterol Nutr. 2004 Jan;38(1):105-6. No abstract available.

PMID:
14676605
46.

Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes.

Türkmen S, Gillessen-Kaesbach G, Meinecke P, Albrecht B, Neumann LM, Hesse V, Palanduz S, Balg S, Majewski F, Fuchs S, Zschieschang P, Greiwe M, Mennicke K, Kreuz FR, Dehmel HJ, Rodeck B, Kunze J, Tinschert S, Mundlos S, Horn D.

Eur J Hum Genet. 2003 Nov;11(11):858-65.

47.
48.

Congenital disorder of glycosylation type 1a in a macrosomic 16-month-old boy with an atypical phenotype and homozygosity of the N216I mutation.

Neumann LM, von Moers A, Kunze J, Blankenstein O, Marquardt T.

Eur J Pediatr. 2003 Oct;162(10):710-3. Epub 2003 Aug 2.

PMID:
12905014
49.

Cerebral manifestations, hemihypertrophy and lymphoedema of one leg in a child with epidermal nevus syndrome (Schimmelpenning-Feuerstein-Mims).

Neumann LM, Scheer I, Kunze J, Stöver B.

Pediatr Radiol. 2003 Sep;33(9):637-40. Epub 2003 Jun 12.

PMID:
12802536
50.

MR imaging features in Marinesco-Sjögren syndrome: severe cerebellar atrophy is not an obligatory finding.

Reinhold A, Scheer I, Lehmann R, Neumann LM, Michael T, Varon R, Von Moers A.

AJNR Am J Neuroradiol. 2003 May;24(5):825-8. Review.

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