-=MAPLE GALAXY=-

50nike9847sx

Clinical application of artificial insemination related factors

thecervica1mucuswereobserved24hrsafterAID. Sexofnewbornwasirive5 a tigated. Results126babieswerebornin123timesofAIDpregnancyand3twinsoc-curred. Amongthemtherewere69malesand57females. Thedifferenceofsexratiobe-tweennaturepregnancyandthisstudyisunremarkable. Meancycleofresultedpregnancyinmixedgroupis2.525: 1_30. It'ssignificantlylongerthanthefrozensemengroup (2.12 Shi 1.20, P. . I. (176d005) Thecervicacircumstanceandspermviabilityincervica1mucus24hafterAIDhavenosignificantrelationwithsexratioofba. bies. ConclusionThesexratioofbornAIDbabiesamongfrozensemengroup, mixedse-mengroupandfreshsemengrouphasnodifference. 2.52cyclesofresultedpregnancyinmixedgroupisobviouslylongerthanothergroups. Keywordsartificialinsemination; cervicalcircumstanceIsexratio (Received :1999-05-28 miserable back: 1990 A n A 0 Cool

J / A glycogen storage disease lipid storage disease o7 Mou 』V Chenzhen Bin Huang Lian Hong Liang Zhang Ping Chen Lianyun cultural and educational purpose of storage of glycogen Product disease with lipid storage disease of the bed and pathological characteristics of Ji. Methods reported 1 patient, Results platform literature review. Describe the clinical and pathological features. Upon the results of disease more common in children or adolescents to women. Progressive or recurrent generalized muscle tension to reduce the t proximal limb weakness or atrophy of a 』L. 』L meat may be associated with a sore. Wei L 』pathological features of a vacuole I fibers appeared diffuse by the King than the amount of muscle fiber type I muscle fibers was significantly and electron microscopy found store of glycogen and lipid droplets in maximus muscle in Victoria. Conclusion solid condition when the patient is limited, can not be biochemical, light and electron microscopy end station D woven bamboo muscle biopsy morphological diagnosis. Key words Glycogen storage disease lipid storage disease} I glycogen storage disease with pathological lipid storage disease is a congenital metabolic myopathy, found in the literature only 3 cases. The author reported one case by light, electron microscopy and confirmed with literature are clinical and pathological features, in order to further investigate the morphological diagnosis of the problem. The clinical data of patients 1 female, 17 years old, was 8 years ago, there was no obvious incentive to lower limb pain, weakness,[link widoczny dla zalogowanych], walking slowly, struggling uphill, no improvement to the traditional Chinese medicine and other treatment. 2 years after the lower limbs can not row 1. Fujian Medical University, Room electron bulk pounds (Fuzhou 350004, China) 2. Fujian Provincial Hospital Internal Medicine 3. Pathological Anatomy,[link widoczny dla zalogowanych], Fujian Medical University, rose to go, the pain got worse, visiting the local hospital to check blood lactate dehydrogenase increased, urine anhydride, creatine were higher, considering polymyositis, to fight infection, hormonal and immune suppression {Bj Jing treatment, symptoms improved and discharged after 40 days. 1 year ago and a sense of lower extremity pain, can not walk long distances, squatting, standing, based upon the symptoms of myositis t 20 days of treatment has improved, well long-term oral prednisone 25mg / d, after self-withdrawal. 3 months before the lower limbs, weakness, increased pain, difficulty climbing stairs, and pain in a double upper limb weakness, the rise of the difficulties,[link widoczny dla zalogowanych], limb muscles become thin. 2O days ago and the emergence of chewing swallowing a cold fever, weakness, choking when eating a t then transferred to Fujian Provincial Hospital for treatment. Hospital examination showed normal development of people,[link widoczny dla zalogowanych], mind clear, soft palate with bilateral activity somewhat less sensitive gag reflex, Shenshe Shaopian right. Wing /
More articles related to topics：