Assmann, B.
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2

O6-1 Loss-of-function mutations in the gene encoding the do..:

Kurian, M.A. ; Zhen, J. ; Cheng, S.-Y....
European Journal of Paediatric Neurology.  13 (2009)  - p. S13 , 2009
 
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3

Rhythmische Lidbewegung beim Kauen und kongenitale Ptosis:

Sabir, H. ; Assmann, B. ; Mayatepek, E..
Monatsschrift Kinderheilkunde.  157 (2008)  11 - p. 1092-1094 , 2008
 
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5

Looking forward—An evidence‐based approach to glutaryl‐CoA ..:

KÖlker, S. ; Burgard, P. ; Okun, J. G....
Journal of Inherited Metabolic Disease.  27 (2004)  6 - p. 921-926 , 2004
 
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6

A new case of CDG‐x with stereotyped dystonic hand movement..:

Prietsch, V. ; Peters, V. ; Hackler, R....
Journal of Inherited Metabolic Disease.  25 (2002)  2 - p. 126-130 , 2002
 
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7

Angle paradigm A new method to measure right parietal dysfu..:

Grunwald, M. ; Ettrich, C. ; Busse, F....
Archives of Clinical Neuropsychology.  17 (2002)  5 - p. 485-496 , 2002
 
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10

Haptische Wahrnehmung und EEG-Veränderungen bei Anorexia ne..:

Grunwald, M. ; Ettrich, C. ; Assmann, B....
Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie.  27 (1999)  4 - p. 241-250 , 1999
 
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11

Magnetic susceptibility, heat capacity, and optical conduct..:

Dumm, M. ; Dressel, M. ; Nicklas, M....
The European Physical Journal B.  6 (1998)  3 - p. 317-322 , 1998
 
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12

Tetra(n‐butyl)ammoniumphthalocyaninato(2–)lithat‐Tetrahydro..:

Latte, Björn ; Aßmann, B. ; Homborg, H.
Zeitschrift für anorganische und allgemeine Chemie.  623 (1997)  8 - p. 1281-1286 , 1997
 
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Dihydropyridmidinase deficiency and congenital microvillous..:

Assmann, B. ; Hoffmann, G. F. ; Wagner, L....
Journal of Inherited Metabolic Disease.  20 (1997)  5 - p. 681-688 , 1997
 
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15

Phosphomannomutase deficiency is the main cause of carbohyd..:

Jaeken, J. ; Artigas, J. ; Barone, R....
Journal of Inherited Metabolic Disease.  20 (1997)  3 - p. 447-449 , 1997
 
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