Lemli

Lem·li

(lem'lē),
Luc, 20th-century U.S. pediatrician. See: Smith-Lemli-Opitz syndrome.
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Marcus Lemli, CEO Savills Germany and head of Savills European investment, says: Globally, the growing amount of capital allocated to real estate in the face of rarefying prime assets is pushing investors from all the world to look beyond their borders, with Asian buyers largely finding a home in Europe.
United Kingdom : Asian investment volumes into Europe to hit 41.2 bn by end of 2017 - more than double 2016 volumes
The clinical description of a dysmorphic syndrome by Smith, Lemli and Opitz in 1964 [1] was linked with abnormal sterol biosynthesis 30 years later.
RSH Smith Lemli Opitz Syndrome: Severe phenotype with ectrodactyly.
Biochemical and genetic diagnosis of Smith-Lemli-Opitz syndrome in South Africa
El Sindrome de Smith-Lemli-Opitz (SSLO) fue descrito en el ano 1964 por Smith, Lemli y Opitz quienes describieron a 3 pacientes de sexo masculino con retraso mental, microcefalia, hipospadia y retraso del desarrollo (1).
Sindrome de Smith-Lemli-Opitz e hipotiroidismo: el primer caso venezolano
Plusieurs varietes sont cultivees, mais six d'entre elles sont les plus repandues, dont achemlal (40%), lemli (25%), azeradj (15%).
Akbou fete l'olive
Smith Lemli Opitz syndrome is related to autism and schizophrenia.
Fossilised Neanderthal matrilineal societies, Neo-Neanderthal hybrids, endosymbiotic actinidic archaea and civilisational diseases
El sindrome de Smith-Lemi-Opitz (SLO) es una enfermedad hereditaria de transmision autosomica recesiva, (1-3) descrita por primera vez en 1964 por sus autores Smith, Lemli y Opitz.
Rehabilitacion oral de un paciente pediatrico con sindrome de Smith-Lemli-Opitz bajo anestesia general ambulatoria
The antispasmodic activity of luteolin has been reported previously (van den Broucke and Lemli, 1983).
Antispasmodic activity of an extract from Plantago lanceolata L. and some isolated compounds
Anita, 18, and Mary have turned the sitting room of their home in Drogheda, Co Louth, into a mini-hospital to care for baby Mary who has the rare genetic condition Smith Lemli Opitz Syndrome.
Miracle of baby Mary; SHE BEATS 60.000-1 SURVIVAL ODDS
He is currently engaged in clinical investigations for Smith Lemli Opitz syndrome, Mevalonate Kinase Deficiency, and phenylketonuria (PKU), disorders which, like Batten disease, are characterized by metabolic deficits and brain involvement.
StemCells, Inc. Receives IRB Approval From Oregon Health & Science University To Begin Phase I Clinical Trial In Batten Disease; First Ever Clinical Trial Using Purified Human Neural Stem Cells

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