Results
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201.
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202.
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A randomised controlled trial of delayed cord clamping in very low birth weight preterm infants. [electronic resource] by
- Rabe, H
- Wacker, A
- Hülskamp, G
- Hörnig-Franz, I
- Schulze-Everding, A
- Harms, E
- Cirkel, U
- Louwen, F
- Witteler, R
- Schneider, H P
Producer: 20010126
In:
European journal of pediatrics vol. 159
Availability: No items available.
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203.
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204.
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Nephropathic cystinosis (CTNS-LSB): construction of a YAC contig comprising the refined critical region on chromosome 17p13. [electronic resource] by
- Peters, U
- Senger, G
- Rählmann, M
- Du Chesne, I
- Stec, I
- Köhler, M R
- Weissenbach, J
- Leal, S M
- Koch, H G
- Deufel, T
- Harms, E
Producer: 19970722
In:
European journal of human genetics : EJHG vol. 5
Availability: No items available.
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205.
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[Fetal nephro-/uropathy: a retrospective analysis of 124 cases seen in the period from 1996 to 2002]. [electronic resource] by
- Bulla, M
- Kuwertz-Bröking, E
- Fründ, S
- Schulze Everding, A
- Louwen, F
- Baez, E
- Steinhard, J
- Brinkmann, O
- August, C
- Harms, E
- Hertle, L
- Kiesel, L
Producer: 20050908
In:
Zeitschrift fur Geburtshilfe und Neonatologie vol. 209
Availability: No items available.
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206.
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207.
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A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If). [electronic resource] by
- Kranz, C
- Denecke, J
- Lehrman, M A
- Ray, S
- Kienz, P
- Kreissel, G
- Sagi, D
- Peter-Katalinic, J
- Freeze, H H
- Schmid, T
- Jackowski-Dohrmann, S
- Harms, E
- Marquardt, T
Producer: 20020103
In:
The Journal of clinical investigation vol. 108
Availability: No items available.
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208.
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Normal clinical outcome in untreated subjects with mild hyperphenylalaninemia. [electronic resource] by
- Weglage, J
- Pietsch, M
- Feldmann, R
- Koch, H G
- Zschocke, J
- Hoffmann, G
- Muntau-Heger, A
- Denecke, J
- Guldberg, P
- Güttler, F
- Möller, H
- Wendel, U
- Ullrich, K
- Harms, E
Producer: 20010614
In:
Pediatric research vol. 49
Availability: No items available.
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209.
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Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy. [electronic resource] by
- Niehues, R
- Hasilik, M
- Alton, G
- Körner, C
- Schiebe-Sukumar, M
- Koch, H G
- Zimmer, K P
- Wu, R
- Harms, E
- Reiter, K
- von Figura, K
- Freeze, H H
- Harms, H K
- Marquardt, T
Producer: 19980423
In:
The Journal of clinical investigation vol. 101
Availability: No items available.
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210.
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Leukocyte adhesion deficiency II syndrome, a generalized defect in fucose metabolism. [electronic resource] by
- Marquardt, T
- Brune, T
- Lühn, K
- Zimmer, K P
- Körner, C
- Fabritz, L
- van der Werft, N
- Vormoor, J
- Freeze, H H
- Louwen, F
- Biermann, B
- Harms, E
- von Figura, K
- Vestweber, D
- Koch, H G
Producer: 19990629
In:
The Journal of pediatrics vol. 134
Availability: No items available.
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