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Items: 1 to 50 of 123

1.

Congenital microcephaly-linked CDK5RAP2 affects eye development.

Zaqout S, Ravindran E, Stoltenburg-Didinger G, Kaindl AM.

Ann Hum Genet. 2019 Jul 29. doi: 10.1111/ahg.12343. [Epub ahead of print]

PMID:
31355417
2.

Microglia damage precedes major myelin breakdown in X-linked adrenoleukodystrophy and metachromatic leukodystrophy.

Bergner CG, van der Meer F, Winkler A, Wrzos C, Türkmen M, Valizada E, Fitzner D, Hametner S, Hartmann C, Pfeifenbring S, Stoltenburg-Didinger G, Brück W, Nessler S, Stadelmann C.

Glia. 2019 Jun;67(6):1196-1209. doi: 10.1002/glia.23598. Epub 2019 Feb 11.

3.

The congenital clubfoot - immunohistological analysis of the extracellular matrix.

Kerling A, Stoltenburg-Didinger G, Grams L, Tegtbur U, Horstmann H, Kück M, Mellerowicz H.

Orthop Res Rev. 2018 Aug 23;10:55-62. doi: 10.2147/ORR.S156449. eCollection 2018.

4.

Immunomodulatory placental-expanded, mesenchymal stromal cells improve muscle function following hip arthroplasty.

Winkler T, Perka C, von Roth P, Agres AN, Plage H, Preininger B, Pumberger M, Geissler S, Hagai EL, Ofir R, Pinzur L, Eyal E, Stoltenburg-Didinger G, Meisel C, Consentius C, Streitz M, Reinke P, Duda GN, Volk HD.

J Cachexia Sarcopenia Muscle. 2018 Oct;9(5):880-897. doi: 10.1002/jcsm.12316. Epub 2018 Sep 19.

5.

The p.S85C-mutation in MATR3 impairs stress granule formation in Matrin-3 myopathy.

Mensch A, Meinhardt B, Bley N, Hüttelmaier S, Schneider I, Stoltenburg-Didinger G, Kraya T, Müller T, Zierz S.

Exp Neurol. 2018 Aug;306:222-231. doi: 10.1016/j.expneurol.2018.05.012. Epub 2018 May 12. No abstract available.

PMID:
29763601
6.

CDK5RAP2 Is Required to Maintain the Germ Cell Pool during Embryonic Development.

Zaqout S, Bessa P, Krämer N, Stoltenburg-Didinger G, Kaindl AM.

Stem Cell Reports. 2017 Feb 14;8(2):198-204. doi: 10.1016/j.stemcr.2017.01.002. Epub 2017 Feb 2.

7.

Synthetic niche to modulate regenerative potential of MSCs and enhance skeletal muscle regeneration.

Pumberger M, Qazi TH, Ehrentraut MC, Textor M, Kueper J, Stoltenburg-Didinger G, Winkler T, von Roth P, Reinke S, Borselli C, Perka C, Mooney DJ, Duda GN, Geißler S.

Biomaterials. 2016 Aug;99:95-108. doi: 10.1016/j.biomaterials.2016.05.009. Epub 2016 May 10.

PMID:
27235995
8.
9.

Mutations in PTRH2 cause novel infantile-onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weakness.

Hu H, Matter ML, Issa-Jahns L, Jijiwa M, Kraemer N, Musante L, de la Vega M, Ninnemann O, Schindler D, Damatova N, Eirich K, Sifringer M, Schrötter S, Eickholt BJ, van den Heuvel L, Casamina C, Stoltenburg-Didinger G, Ropers HH, Wienker TF, Hübner C, Kaindl AM.

Ann Clin Transl Neurol. 2014 Dec;1(12):1024-35. doi: 10.1002/acn3.149. Epub 2014 Dec 3.

10.

Phenotype of matrin-3-related distal myopathy in 16 German patients.

Müller TJ, Kraya T, Stoltenburg-Didinger G, Hanisch F, Kornhuber M, Stoevesandt D, Senderek J, Weis J, Baum P, Deschauer M, Zierz S.

Ann Neurol. 2014 Nov;76(5):669-80. doi: 10.1002/ana.24255. Epub 2014 Sep 16.

PMID:
25154462
11.

Eosinophils in hereditary and inflammatory myopathies.

Schröder T, Fuchss J, Schneider I, Stoltenburg-Didinger G, Hanisch F.

Acta Myol. 2013 Dec;32(3):148-53.

12.

Noninvasive monitoring of training induced muscle adaptation with 31P-MRS: fibre type shifts correlate with metabolic changes.

Hoff E, Brechtel L, Strube P, Konstanczak P, Stoltenburg-Didinger G, Perka C, Putzier M.

Biomed Res Int. 2013;2013:417901. doi: 10.1155/2013/417901. Epub 2013 Jul 15.

13.

Polymyositis with cytochrome C oxidase negative fibers--a pathological and clinical challenge.

Siepmann T, Tesch M, Krause F, Illigens BM, Stoltenburg-Didinger G.

Ann Diagn Pathol. 2013 Apr;17(2):183-6. doi: 10.1016/j.anndiagpath.2012.10.004. Epub 2012 Nov 20.

PMID:
23181976
14.

CDK5RAP2 expression during murine and human brain development correlates with pathology in primary autosomal recessive microcephaly.

Issa L, Kraemer N, Rickert CH, Sifringer M, Ninnemann O, Stoltenburg-Didinger G, Kaindl AM.

Cereb Cortex. 2013 Sep;23(9):2245-60. doi: 10.1093/cercor/bhs212. Epub 2012 Jul 17.

PMID:
22806269
15.

Systemic inflammation disrupts the developmental program of white matter.

Favrais G, van de Looij Y, Fleiss B, Ramanantsoa N, Bonnin P, Stoltenburg-Didinger G, Lacaud A, Saliba E, Dammann O, Gallego J, Sizonenko S, Hagberg H, Lelièvre V, Gressens P.

Ann Neurol. 2011 Oct;70(4):550-65. doi: 10.1002/ana.22489. Epub 2011 Jul 27.

PMID:
21796662
16.

Time course of skeletal muscle regeneration after severe trauma.

Winkler T, von Roth P, Matziolis G, Schumann MR, Hahn S, Strube P, Stoltenburg-Didinger G, Perka C, Duda GN, Tohtz SV.

Acta Orthop. 2011 Feb;82(1):102-11. doi: 10.3109/17453674.2010.539498. Epub 2010 Dec 13.

17.

In utero development of symmetric thalamic and brainstem necrosis in a preterm hydropic stillborn.

Szekessy DP, Bamberg C, Blechschmidt C, Kaindl AM, Stoltenburg-Didinger G.

Clin Neuropathol. 2010 Nov-Dec;29(6):365-71.

PMID:
21073840
18.

Regionalized pathology correlates with augmentation of mtDNA copy numbers in a patient with myoclonic epilepsy with ragged-red fibers (MERRF-syndrome).

Brinckmann A, Weiss C, Wilbert F, von Moers A, Zwirner A, Stoltenburg-Didinger G, Wilichowski E, Schuelke M.

PLoS One. 2010 Oct 20;5(10):e13513. doi: 10.1371/journal.pone.0013513.

19.

Cerebral expression of neuroglobin and cytoglobin after deep hypothermic circulatory arrest in neonatal piglets.

Schubert S, Gerlach F, Stoltenburg-Didinger G, Burmester T, Hankeln T, Boettcher W, Wehsack A, Hübler M, Berger F, Abdul-Khaliq H.

Brain Res. 2010 Oct 14;1356:1-10. doi: 10.1016/j.brainres.2010.08.005. Epub 2010 Aug 10.

PMID:
20705062
20.

Progressive multifocal leukoencephalopathy in a patient with undifferentiated systemic vasculitis and bilateral acute retinal necrosis.

Feist E, Stoltenburg-Didinger G, Dörner T, Burmester GR, Pleyer U.

Clin Exp Rheumatol. 2009 Jan-Feb;27(1 Suppl 52):S139-40. No abstract available.

PMID:
19646359
21.

[Dermatomyositis].

Stoltenburg-Didinger G, Genth E.

Z Rheumatol. 2009 Jun;68(4):287-94. doi: 10.1007/s00393-008-0398-y. Review. German.

PMID:
19330338
22.

In vivo visualization of locally transplanted mesenchymal stem cells in the severely injured muscle in rats.

Winkler T, von Roth P, Schuman MR, Sieland K, Stoltenburg-Didinger G, Taupitz M, Perka C, Duda GN, Matziolis G.

Tissue Eng Part A. 2008 Jul;14(7):1149-60. doi: 10.1089/tea.2007.0179.

PMID:
18433314
23.

Novel RYR1 missense mutation causes core rod myopathy.

von der Hagen M, Kress W, Hahn G, Brocke KS, Mitzscherling P, Huebner A, Müller-Reible C, Stoltenburg-Didinger G, Kaindl AM.

Eur J Neurol. 2008 Apr;15(4):e31-2. doi: 10.1111/j.1468-1331.2008.02094.x. Epub 2008 Feb 26. No abstract available.

PMID:
18312400
24.

Differential activation of mononuclear phagocytes in cerebellar malformation associated with Walker-Warburg syndrome.

Ulfig N, Steinbrecher A, Stoltenburg-Didinger G, Rezaie P.

Neuropathology. 2008 Jun;28(3):333-40. Epub 2007 Dec 5.

PMID:
18069971
25.

Progressive multicystic encephalopathy: is there more than hypoxia-ischemia?

Garten L, Hueseman D, Stoltenburg-Didinger G, Felderhoff-Mueser U, Weizsaecker K, Scheer I, Boltshauser E, Obladen M.

J Child Neurol. 2007 May;22(5):645-9.

PMID:
17690077
26.

Lethal fetal and early neonatal presentation of adenylosuccinate lyase deficiency: observation of 6 patients in 4 families.

Mouchegh K, Zikánová M, Hoffmann GF, Kretzschmar B, Kühn T, Mildenberger E, Stoltenburg-Didinger G, Krijt J, Dvoráková L, Honzík T, Zeman J, Kmoch S, Rossi R.

J Pediatr. 2007 Jan;150(1):57-61.e2.

PMID:
17188615
27.

Painful enlargement of the calf muscles in limb girdle muscular dystrophy type 2B (LGMD2B) with a novel compound heterozygous mutation in DYSF.

Diers A, Carl M, Stoltenburg-Didinger G, Vorgerd M, Spuler S.

Neuromuscul Disord. 2007 Feb;17(2):157-62. Epub 2006 Nov 28.

PMID:
17129727
28.

Selenoprotein N muscular dystrophy: differential diagnosis for early-onset limited mobility of the spine.

Sponholz S, von der Hagen M, Hahn G, Seifert J, Richard P, Stoltenburg-Didinger G, Ferreiro A, Kaindl AM.

J Child Neurol. 2006 Apr;21(4):316-20.

PMID:
16900928
29.

Sudden infant death syndrome (SIDS)--standardised investigations and classification: recommendations.

Bajanowski T, Vege A, Byard RW, Krous HF, Arnestad M, Bachs L, Banner J, Blair PS, Borthne A, Dettmeyer R, Fleming P, Gaustad P, Gregersen M, Grøgaard J, Holter E, Isaksen CV, Jorgensen JV, de Lange C, Madea B, Moore I, Morland J, Opdal SH, Råsten-Almqvist P, Schlaud M, Sidebotham P, Skullerud K, Stoltenburg-Didinger G, Stray-Pedersen A, Sveum L, Rognum TO.

Forensic Sci Int. 2007 Jan 17;165(2-3):129-43. Epub 2006 Jun 27. Review.

PMID:
16806765
30.

A 19-year-old male with generalized seizures, unconsciousness and a deviation of gaze.

Fischer L, Korfel A, Stoltenburg-Didinger G, Ransco C, Thiel E.

Brain Pathol. 2006 Apr;16(2):185-6, 187.

PMID:
16768760
31.

Three-dimensional ultrasonographic reslicing of the fetal brain to assist prenatal diagnosis of central nervous system anomalies.

Kalache KD, Eder K, Esser T, Proquitté H, Stoltenburg-Didinger G, Hartung JP, Bamberg C.

J Ultrasound Med. 2006 Apr;25(4):509-14.

PMID:
16567440
32.

Mice lacking the nuclear pore complex protein ALADIN show female infertility but fail to develop a phenotype resembling human triple A syndrome.

Huebner A, Mann P, Rohde E, Kaindl AM, Witt M, Verkade P, Jakubiczka S, Menschikowski M, Stoltenburg-Didinger G, Koehler K.

Mol Cell Biol. 2006 Mar;26(5):1879-87.

33.

A 62-year-old man with chronic pyothorax.

Loddenkemper C, Hoecht S, Anagnostopoulos I, Heine B, Stoltenburg-Didinger G, Stein H.

Brain Pathol. 2005 Oct;15(4):371-3.

PMID:
16389950
34.

Large-dose pretreatment with methylprednisolone fails to attenuate neuronal injury after deep hypothermic circulatory arrest in a neonatal piglet model.

Schubert S, Stoltenburg-Didinger G, Wehsack A, Troitzsch D, Boettcher W, Huebler M, Redlin M, Kanaan M, Meissler M, Lange PE, Abdul-Khaliq H.

Anesth Analg. 2005 Nov;101(5):1311-8.

PMID:
16243986
35.

Megacolon in adulthood after surgical treatment of Hirschsprung's disease in early childhood.

Werner CR, Stoltenburg-Didinger G, Weidemann H, Benckert C, Schmidtmann M, van der Voort IR, Andresen V, Klapp BF, Neuhaus P, Wiedenmann B, Mönnikes H.

World J Gastroenterol. 2005 Sep 28;11(36):5742-5.

36.

The HIV protease inhibitors saquinavir, ritonavir, and nelfinavir induce apoptosis and decrease barrier function in human intestinal epithelial cells.

Bode H, Lenzner L, Kraemer OH, Kroesen AJ, Bendfeldt K, Schulzke JD, Fromm M, Stoltenburg-Didinger G, Zeitz M, Ullrich R.

Antivir Ther. 2005;10(5):645-55.

PMID:
16152758
37.

Limb girdle muscular dystrophy type 2I caused by a novel missense mutation in the FKRP gene presenting as acute virus-associated myositis in infancy.

von der Hagen M, Kaindl AM, Koehler K, Mitzscherling P, Häusler HJ, Stoltenburg-Didinger G, Huebner A.

Eur J Pediatr. 2006 Jan;165(1):62-3. Epub 2005 Sep 6. No abstract available.

PMID:
16143867
38.

Homozygous microdeletion of chromosome 4q11-q12 causes severe limb-girdle muscular dystrophy type 2E with joint hyperlaxity and contractures.

Kaindl AM, Jakubiczka S, Lücke T, Bartsch O, Weis J, Stoltenburg-Didinger G, Aksu F, Oexle K, Koehler K, Huebner A.

Hum Mutat. 2005 Sep;26(3):279-80.

PMID:
16088906
39.

The ultrastructure of peripheral nerve, motor end-plate and skeletal muscle in patients suffering from spinal muscular atrophy with respiratory distress type 1 (SMARD1).

Diers A, Kaczinski M, Grohmann K, Hübner C, Stoltenburg-Didinger G.

Acta Neuropathol. 2005 Sep;110(3):289-97. Epub 2005 Jul 16.

PMID:
16025284
40.

Delayed or late-onset type II glycogenosis with globular inclusions.

Sharma MC, Schultze C, von Moers A, Stoltenburg-Didinger G, Shin YS, Podskarbi T, Isenhardt K, Tews DS, Goebel HH.

Acta Neuropathol. 2005 Aug;110(2):151-7. Epub 2005 Jun 29.

PMID:
15986226
41.

Demonstration of identical clonal derivation in a case of "oculocerebral" lymphoma.

Coupland SE, Hummel M, Stein H, Willerding G, Jahnke K, Stoltenburg-Didinger G.

Br J Ophthalmol. 2005 Feb;89(2):238-9. No abstract available.

42.

Increased mRNA expression of tissue inhibitors of metalloproteinase-1 and -2 in Duchenne muscular dystrophy.

von Moers A, Zwirner A, Reinhold A, Brückmann O, van Landeghem F, Stoltenburg-Didinger G, Schuppan D, Herbst H, Schuelke M.

Acta Neuropathol. 2005 Mar;109(3):285-93. Epub 2004 Dec 23.

PMID:
15616792
43.

Missense mutations of ACTA1 cause dominant congenital myopathy with cores.

Kaindl AM, Rüschendorf F, Krause S, Goebel HH, Koehler K, Becker C, Pongratz D, Müller-Höcker J, Nürnberg P, Stoltenburg-Didinger G, Lochmüller H, Huebner A.

J Med Genet. 2004 Nov;41(11):842-8. No abstract available.

44.

Giant intracerebral choroid plexus calcification.

Picht T, Stendel R, Stoltenburg-Didinger G, Brock M.

Acta Neurochir (Wien). 2004 Nov;146(11):1259-61. Epub 2004 Jun 28.

PMID:
15503189
45.

Brain-IL-1 beta triggers astrogliosis through induction of IL-6: inhibition by propranolol and IL-10.

Woiciechowsky C, Schöning B, Stoltenburg-Didinger G, Stockhammer F, Volk HD.

Med Sci Monit. 2004 Sep;10(9):BR325-30. Epub 2004 Aug 20.

PMID:
15328477
46.

Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1).

Grohmann K, Rossoll W, Kobsar I, Holtmann B, Jablonka S, Wessig C, Stoltenburg-Didinger G, Fischer U, Hübner C, Martini R, Sendtner M.

Hum Mol Genet. 2004 Sep 15;13(18):2031-42. Epub 2004 Jul 21.

PMID:
15269181
47.

Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease.

Uhlenberg B, Schuelke M, Rüschendorf F, Ruf N, Kaindl AM, Henneke M, Thiele H, Stoltenburg-Didinger G, Aksu F, Topaloğlu H, Nürnberg P, Hübner C, Weschke B, Gärtner J.

Am J Hum Genet. 2004 Aug;75(2):251-60. Epub 2004 Jun 10. Erratum in: Am J Hum Genet. 2004 Oct;5(4):737.

48.

The cerebral cortex in fetal Down syndrome.

Unterberger U, Lubec G, Dierssen M, Stoltenburg-Didinger G, Farreras JC, Budka H.

J Neural Transm Suppl. 2003;(67):159-63.

PMID:
15068248
49.

The endothelin system in Morris hepatoma-7777: an endothelin receptor antagonist inhibits growth in vitro and in vivo.

Pfab T, Stoltenburg-Didinger G, Trautner C, Godes M, Bauer C, Hocher B.

Br J Pharmacol. 2004 Jan;141(2):215-22. Epub 2003 Dec 8.

50.

Chronic lumbar epidural haematoma presenting with acute paraparesis.

Stendel R, Danne M, Schulte T, Stoltenburg-Didinger G, Brock M.

Acta Neurochir (Wien). 2003 Nov;145(11):1015-8; discussion 1018. Review.

PMID:
14628208

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