𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Biliary atresia and Kabuki syndrome: Another case with long-term follow-up

✍ Scribed by Selicorni, Angelo ;Colombo, Carla ;Bonato, Sara ;Milani, Donatella ;Giunta, Anna Maria ;Bedeschi, Maria Francesca

Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
33 KB
Volume
100
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Long-term follow-up of Lambert-Eaton syn
Long-term follow-up of Lambert-Eaton syndrome treated with intravenous immunoglobulin
✍ Salomon Muchnik; Adriana S. Losavio; Alfredo Vidal; Leila Cura; Claudio Mazia πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 194 KB πŸ‘ 2 views

Recent reports have shown that patients with Lambert-Eaton myasthenic syndrome (LEMS) improve transiently after high-dose intravenous immunoglobulin (IVIG) administration. Information about the usefulness of IVIG for long-term treatment is rather scanty. Our findings demonstrate the efficacy of mont

Follow-up study of Wiedemann-Rautenstrau
Follow-up study of Wiedemann-Rautenstrauch syndrome: Long-term survival and comparison with Rautenstrauch's patient β€œG”
✍ Humberto Arboleda; Gonzalo Arboleda πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 250 KB

## Abstract ## BACKGROUND Wiedemann‐Rautenstrauch syndrome (WRS) characterizes a neonatal progeroid entity. In the last 30 years, 28 cases have been reported. In most cases of WRS, survival is short and long‐term studies are impossible. ## CASE In the present report, we describe a patient with W

Zimmermann-Laband syndrome in an adult.
Zimmermann-Laband syndrome in an adult. Long-term follow-up of a patient with vascular and cardiac complications
✍ Robertson, Stephen P.; Lipp, Harry; Bankier, Agnes πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 37 KB πŸ‘ 2 views

Zimmermann-Laband syndrome (ZLS) is characterised by findings of coarse facial appearance, hepatosplenomegaly, and hirsutism often first observed in infancy, followed by the evolution during childhood of gingival fibromatosis, small joint hyperextensibility, and hypoplasia of the finger-and toenails