Röhrig D[au] - Search Results

Year	Number of Results
1972	1
1984	1
1993	3
1994	1
1995	2
1997	1
1998	2
1999	1
2019	1
2022	0

1

Laminar specificity of oscillatory coherence in the auditory cortex.

García-Rosales F, Röhrig D, Weineck K, Röhm M, Lin YH, Cabral-Calderin Y, Kössl M, Hechavarria JC. García-Rosales F, et al. Among authors: rohrig d. Brain Struct Funct. 2019 Nov;224(8):2907-2924. doi: 10.1007/s00429-019-01944-3. Epub 2019 Aug 27. Brain Struct Funct. 2019. PMID: 31456067

2

[Spinal muscular atrophy in childhood. Possibilities and limits of clinical and molecular genetic diagnosis].

Zerres K, Rudnik-Schöneborn S, Röhrig D, Wirth B. Zerres K, et al. Among authors: rohrig d. Monatsschr Kinderheilkd. 1993 Nov;141(11):848-54. Monatsschr Kinderheilkd. 1993. PMID: 8283989 Review. German.

3

Pregnancy and delivery in Charcot-Marie-Tooth disease type 1.

Rudnik-Schöneborn S, Röhrig D, Nicholson G, Zerres K. Rudnik-Schöneborn S, et al. Among authors: rohrig d. Neurology. 1993 Oct;43(10):2011-6. doi: 10.1212/wnl.43.10.2011. Neurology. 1993. PMID: 8413959

4

Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studies.

Wirth B, Voosen B, Röhrig D, Knapp M, Piechaczek B, Rudnik-Schöneborn S, Zerres K. Wirth B, et al. Among authors: rohrig d. Genomics. 1993 Jan;15(1):113-8. doi: 10.1006/geno.1993.1018. Genomics. 1993. PMID: 8432521

5

Obstetric aspects in women with facioscapulohumeral muscular dystrophy, limb-girdle muscular dystrophy, and congenital myopathies.

Rudnik-Schöneborn S, Glauner B, Röhrig D, Zerres K. Rudnik-Schöneborn S, et al. Among authors: rohrig d. Arch Neurol. 1997 Jul;54(7):888-94. doi: 10.1001/archneur.1997.00550190076017. Arch Neurol. 1997. PMID: 9236578

6

Different patterns of obstetric complications in myotonic dystrophy in relation to the disease status of the fetus.

Rudnik-Schöneborn S, Nicholson GA, Morgan G, Röhrig D, Zerres K. Rudnik-Schöneborn S, et al. Among authors: rohrig d. Am J Med Genet. 1998 Dec 4;80(4):314-21. Am J Med Genet. 1998. PMID: 9856556

7

Exclusion of the gene locus for spinal muscular atrophy on chromosome 5q in a family with infantile olivopontocerebellar atrophy (OPCA) and anterior horn cell degeneration.

Rudnik-Schöneborn S, Wirth B, Röhrig D, Saule H, Zerres K. Rudnik-Schöneborn S, et al. Among authors: rohrig d. Neuromuscul Disord. 1995 Jan;5(1):19-23. doi: 10.1016/0960-8966(94)e0025-4. Neuromuscul Disord. 1995. PMID: 7719136

8

Autosomal recessive proximal spinal muscular atrophy in 101 sibs out of 48 families: clinical picture, influence of gender, and genetic implications.

Rudnik-Schöneborn S, Röhrig D, Morgan G, Wirth B, Zerres K. Rudnik-Schöneborn S, et al. Among authors: rohrig d. Am J Med Genet. 1994 May 15;51(1):70-6. doi: 10.1002/ajmg.1320510115. Am J Med Genet. 1994. PMID: 8030672

9

Increased risk for abnormal placentation in women affected by myotonic dystrophy.

Rudnik-Schöneborn S, Röhrig D, Zerres K. Rudnik-Schöneborn S, et al. Among authors: rohrig d. J Perinat Med. 1998;26(3):192-5. doi: 10.1515/jpme.1998.26.3.192. J Perinat Med. 1998. PMID: 9773377

10

Evaluation of the facioscapulohumeral muscular dystrophy (FSHD1) phenotype in correlation to the concurrence of 4q35 and 10q26 fragments.

Köhler J, Röhrig D, Bathke KD, Koch MC. Köhler J, et al. Among authors: rohrig d. Clin Genet. 1999 Feb;55(2):88-94. doi: 10.1034/j.1399-0004.1999.550204.x. Clin Genet. 1999. PMID: 10189085

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